Identity
- Trade Name
- CARDINAL HEALTH FDA UDI
- Generic Name
- Basic male condom, Hevea-latex FDA UDI
- Device Name
- RETINAL PACK FDA UDI
- Model / Reference
- SEY35REM16 FDA UDI
- Description
- RETINAL PACK FDA UDI
Identifiers
- Catalog Number
- SEY35REM16 FDA UDI
- Primary DI / UDI-DI
- 10197106875254 FDA UDI
- FDA Product Code
- OJA FDA UDI
- GMDN Term
- Basic male condom, Hevea-latex FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.5440 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
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
Yes
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
Yes
FDA UDI
Category: Basic male condom, Hevea-latex
Cardinal Health by Cardinal Health 200, LLC — Class II — 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 II | Pending data |
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Manufacturer
- Manufacturer
- Cardinal Health 200, LLC
Sources (1)
- FDA UDI dbe56608-1b4c-4fc4-8362-dbd280670bf7 34 fields · synced Jun 8, 2026