Identity
- Trade Name
- NAMIC FDA UDI
- Generic Name
- Angiography kit FDA UDI
- Device Name
- NAMIC Convenience Kit FDA UDI
- Model / Reference
- 6561028971 FDA UDI
- Description
- NAMIC Convenience Kit FDA UDI
Identifiers
- Primary DI / UDI-DI
- H96565610289710 FDA UDI
- GMDN Term
- Angiography kit FDA UDI
Classification
- 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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Angiography kit
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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 | N/A | Pending data |
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Manufacturer
- Manufacturer
- Navilyst Medical, Inc.
Sources (1)
- FDA UDI 89a5671c-a434-4c99-a089-ca64f4b4e3ee 34 fields · synced Jul 31, 2026