Identity
- Trade Name
- FAAC-4 - UP Facilities - 4-Shelf Cabinet FDA UDI
- Generic Name
- Cardiopulmonary resuscitation mask, single-use FDA UDI
- Device Name
- FAAC-4 - UP Facilities - 4-Shelf Cabinet FDA UDI
- Model / Reference
- K612-167 FDA UDI
- Description
- FAAC-4 - UP Facilities - 4-Shelf Cabinet FDA UDI
Identifiers
- Catalog Number
- K612-167 FDA UDI
- Primary DI / UDI-DI
- 00766588121673 FDA UDI
- FDA Product Code
- LRR FDA UDIKGX FDA UDIIMD FDA UDICBP FDA UDIEFQ FDA UDI
- GMDN Term
- Cardiopulmonary resuscitation mask, single-use FDA UDI
Classification
- Device Class
- N FDA UDI
- Regulation Number
- 880.5240 FDA UDI890.5710 FDA UDI868.5870 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
No
FDA UDI
Convenience Kit
No
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
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: First aid kit, medicatedAdhesive bandageNon-woven gauze padNon-rebreathing valve, single-use
FAAC-4 - UP Facilities - 4-Shelf Cabinet by Certified Safety Manufacturing, Inc. — 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
- Certified Safety Manufacturing, Inc.
Sources (1)
- FDA UDI 10b3608c-9910-4ecf-a466-fc0a42a6d524 35 fields · synced Jun 1, 2026