Identity
- Trade Name
- Corning FDA UDI
- Generic Name
- Blood/tissue storage/culture container FDA UDI
- Device Name
- Corning CellCube 25-Layer module Polystyrene CellBIND treated Growth Surface with Polycarbonate end plates and Silicone tubing, with Female inlet, Male outlet FDA UDI
- Model / Reference
- 11210 FDA UDI
- Description
- Corning CellCube 25-Layer module Polystyrene CellBIND treated Growth Surface with Polycarbonate end plates and Silicone tubing, with Female inlet, Male outlet FDA UDI
Identifiers
- Catalog Number
- 11210 FDA UDI
- Primary DI / UDI-DI
- H108112101 FDA UDI
- FDA Product Code
- KJA FDA UDI
- GMDN Term
- Blood/tissue storage/culture container FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 864.2240 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Blood/tissue storage/culture container
Corning by Corning Incorporated — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Corning Incorporated
Sources (1)
- FDA UDI 5594a9e7-30b7-4918-92ce-c1bc86ecd5f4 35 fields · synced May 29, 2026