Identity
- Trade Name
- Unipower FDA UDI
- Generic Name
- Portable/mobile rechargeable battery pack FDA UDI
- Model / Reference
- B11694 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00817392024299 FDA UDI
- FDA Product Code
- LDD FDA UDI
- GMDN Term
- Portable/mobile rechargeable battery pack FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.5300 FDA UDI
- Commercial Distribution
- Not 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
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Unipower by Unipower Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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
- Unipower Corp.
Sources (1)
- FDA UDI 67543d15-e8b8-49c8-9382-cbae069a1a6a 33 fields · synced May 31, 2026