Paragard T 380a Intrauterine Device
Product Images NDC 59365-5129

Product Visual Gallery

This gallery contains 17 technical images submitted to the FDA as part of the official labeling for Paragard T 380a (NDC 59365-5129). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Coopersurgical, Inc., these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

FDA Label Image

Figure 1 (Par07 0000 01)

Illustration diagram of the ParaGard T 380A intrauterine device packaging showing labeled components including the loading tip, paragard, flange, tray, button, starting line, handle, and clear cover.*

FDA Label Image

Figure 2 (Par07 0000 02)

An anatomical illustration of the ParaGard T 380A intrauterine device showing its T-shaped structure. The diagram labels the copper wire coiled around the horizontal arms, the copper collar, the vertical stem, and the monofilament threads extending from the bottom.*

FDA Label Image

Figure 3 (Par07 0000 03)

An instructional illustration showing the handling and loading process of the ParaGard T 380A intrauterine device (IUD) into its insertion tube. Hands are depicted holding the device and the applicator with close-up insets highlighting specific mechanism details, including device placement and lock positions for accurate insertion.*

FDA Label Image

Figure 4 (Par07 0000 04)

Illustration showing detailed internal and external views of the ParaGard T 380A intrauterine device (IUD) delivery system, including close-ups of the mechanism for device placement and release. The diagram highlights components involved in the insertion process of the copper IUD.*

FDA Label Image

Figure 5 (Par07 0000 05)

An instructional line drawing depicting the ParaGard T 380A intrauterine device (IUD) inside a narrow applicator tube, showing the shape and positioning of the IUD within the insertion device.*

FDA Label Image

Figure 6 (Par07 0000 06)

Illustration showing the ParaGard T 380A intrauterine device (IUD) and its inserter tool positioned in a molded tray. An arrow indicates assembly of the IUD onto the inserter, depicting device preparation for intrauterine insertion.*

FDA Label Image

Figure 7 (Par07 0000 07)

An instructional diagram showing the insertion process of the ParaGard T 380A intrauterine device (IUD). The illustration depicts the device being positioned inside the uterus with a focus on the inserter handle, including a close-up inset highlighting the positioning of the string guide during placement.*

FDA Label Image

Figure 8 (Par07 0000 08)

Illustration showing how to hold and remove the ParaGard T 380A intrauterine device (IUD) inserter from the uterus. The hand grips the inserter while instructions indicate sliding the button back to release threads for removal.*

FDA Label Image

Figure 9 (Par07 0000 09)

An instructional diagram showing an intrauterine device (IUD) placed inside the uterus. The image highlights the trimming of device threads to ensure they protrude 3 to 4 centimeters into the vagina, with a labeled measurement for proper thread length adjustment.*

FDA Label Image

Mr Caution Image (Par07 0000 10)

FDA Label Image

Figure (Par07 0000 11)

An instructional diagram showing the components and dimensions of the ParaGard T 380A intrauterine device. The device measures 32 mm in width and 36 mm in height, featuring labeled parts including the copper wire, vertical stem, copper collar, horizontal arm, and monofilament threads.*

FDA Label Image

Figure (Par07 0000 12)

An instructional diagram illustrating the components of the ParaGard T 380A intrauterine device (IUD) packaging tray. Labeled parts include the loading tip, Paragard IUD, flange, tray, starting line, button, handle, and clear cover, showing arrangement and features within the packaging tray.*

FDA Label Image

Figure (Par07 0000 13)

Illustration of the ParaGard T 380A intrauterine device (IUD) showing its T-shape with measurements indicating approximate dimensions of 1.26 inches in width and 1.42 inches in height. The image includes a disclaimer that the device is shown for illustrative purposes only and is not actual size.*

FDA Label Image

Figure (Par07 0000 14)

An instructional diagram depicting pregnancy rates associated with different contraceptive methods. It features a vertical scale ranging from fewer than 1 pregnancy per 100 women per year at the top to 85 or more pregnancies per 100 women per year at the bottom. Various birth control methods are categorized along this scale from most to least effective, including implants, injections, intrauterine devices, sterilization, birth control pills, skin patch, vaginal rings with hormones, condoms, diaphragm, spermicides, withdrawal, and no birth control.*

FDA Label Image

Figure (Par07 0000 15)

An anatomical illustration showing the ParaGard T 380A intrauterine device positioned inside the uterus. The diagram labels the uterus, vagina, ParaGard device, and its threads extending into the vaginal canal, depicting the correct placement of the copper IUD.*

FDA Label Image

Figure (Par07 0000 16)

An instructional diagram showing the female reproductive anatomy with a hand feeling for the short threads attached to the ParaGard T 380A intrauterine device (IUD). The threads are labeled and highlighted to indicate how the user should feel for them with a finger.*

FDA Label Image

Principal Display Panel – Carton Label (Par07 0000 17)

Packaging label for ParaGard T 380A intrauterine copper contraceptive, a human prescription drug by CooperSurgical, Inc. The label shows 1 unit of the intrauterine device containing 313.4 mg of copper. The label includes the product name, description, a device illustration, and regulatory information, emphasizing its intrauterine use.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.