Identity
- Trade Name
- DC Safety FDA UDI
- Generic Name
- Medical bag FDA UDI
- Device Name
- SWK FDA UDI
- Model / Reference
- ARF72 AU101 XX FDA UDI
- Description
- SWK FDA UDI
Identifiers
- Catalog Number
- ARF72 AU101 XX FDA UDI
- Primary DI / UDI-DI
- 00816058013059 FDA UDI
- FDA Product Code
- LRR FDA UDI
- GMDN Term
- Medical bag FDA UDI
Classification
- Device Class
- N FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
FDA UDI
Over-the-Counter
Yes
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
No
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Medical bag
DC Safety by DC Safety Sales — Class N — 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 N | Pending data |
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Manufacturer
- Manufacturer
- DC Safety Sales
Sources (1)
- FDA UDI fee39d6f-671d-4a52-94a7-62c5aa72fb19 35 fields · synced May 30, 2026