Identity
- Trade Name
- Costar FDA UDI
- Generic Name
- Blood/tissue storage/culture container FDA UDI
- Device Name
- Transwell, OI, 75MM, 3.0, PC,NT,OX,7165 btm,htd bd,S,IND,1/48 FDA UDI
- Model / Reference
- 7474 FDA UDI
- Description
- Transwell, OI, 75MM, 3.0, PC,NT,OX,7165 btm,htd bd,S,IND,1/48 FDA UDI
Identifiers
- Catalog Number
- 7474 FDA UDI
- Primary DI / UDI-DI
- H10874741 FDA UDI
- FDA Product Code
- KIZ 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
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Blood/tissue storage/culture container
Costar 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 2ec3049f-01a6-4026-89cc-423fc021a1e5 35 fields · synced Jun 7, 2026