Figure 1 (Maci 01)
Maci Implant
Product Images NDC 69866-1030
View Photos of Packaging, Regulatory Labels, and Product Appearance
Product Visual Gallery
This gallery contains 10 technical images submitted to the FDA as part of the official labeling for Maci (NDC 69866-1030). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Vericel Corporation, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.
Figure 2 (Maci 02)
Figure 3 (Maci 03)
Figure 4 (Maci 04)
Dish Label (Maci 05)
This is a description of a medical product called MACI® by Vericel Corporation. It involves the use of autologous cultured chondrocytes on porcine collagen membrane to repair damaged cartilage. The label includes patient and product identification numbers, lot number, and expiry date.*
Outer Bag Label (Maci 06)
This is a package containing an implant designed for autologous use only. The implant is composed of autologous cultured chondrocytes on a porcine collagen membrane. The package does not contain preservatives, and it should not be used if the patient has known allergies to gentamicin or other aminoglycosides, or products of porcine or bovine origin. The package has a lot number and an expiration date. The implant density should be at least 500,000 cells per cm?. The package is manufactured by Vericel Corporation and has a License number of 2010.*
Shipper Label (Maci 07)
This is a package of MACI implant which is meant for autologous use only. It contains autologous cultured chondrocytes on a Type VII collagen membrane. This package does not contain any preservatives and is not evaluated for infectious substances. It is not safe for patients allergic to gentamicin, other aminoglycosides or products of porcine or bovine origin. This package is meant for one-time use only and it's labeled with the patient ID #, lot #, and expiration date. The package insert must be consulted for prescribing information and administration instructions. The product is manufactured by Vericel Corporation in Cambridge, MA, and it is categorized with NDC 69866-1030-5.*
Dish Label (Maci 08)
This is a label for a medical product called MACI, produced by Vericel Corporation in Cambridge, Massachusetts, USA, containing autologous cultured chondrocytes on porcine collagen membrane. The label includes patient ID number, lot number, expiry date, and a license number. The product is only for use in autologous treatments. The rest of the text contains barcode numbers and label identification numbers.*
Outer Bag Label (Maci 09)
This package contains MACI implants consisting of autologous cultured chondrocytes on a resorbable collagen membrane. It is intended for autologous use only and has not been evaluated for infectious substances. The product must not be used in patients who have known allergies to gentamicin, other aminoglycosides, porcine or bovine origin products. The package contains two implants with a size of 3x5 cm each, with a density of at least 500,000 cells per cm2. The lot number is BB00000-00, and the expiration date is January 01, 2022. Patient ID # is 000000. Full instructions for administration are available in the package insert. Store the implant package at room temperature, avoiding freezing.*
Shipper Label (Maci 10)
This is a package of two MACI implants, used for autologous purposes only, containing cultured chondrocytes on a collagen membrane. The implants have not been evaluated for infectious substances and do not contain any preservatives. Patients with known allergies to certain substances should not use this product. The package comes with a lot number, expiration date, and patient ID, and the full prescribing information and administration instructions can be found in the package insert. MACI is a registered trademark of Vericel Corporation.*
* 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.
