Identity
- Trade Name
- LIFEPAK 1000 LiMnO2 non rechargeable battery FDA UDI
- Generic Name
- Primary battery FDA UDI
- Device Name
- ASSEMBLY BATTERY REPLACEMENT KIT FDA UDI
- Model / Reference
- 11141 FDA UDI
- Description
- ASSEMBLY BATTERY REPLACEMENT KIT FDA UDI
Identifiers
- Catalog Number
- 11141-000100 FDA UDI
- Primary DI / UDI-DI
- 00885074503592 FDA UDI
- FDA Product Code
- MKJ FDA UDI
- GMDN Term
- Primary battery FDA UDI
Classification
- Device Class
- Class III FDA UDI
- Regulation Number
- 870.5310 FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
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
Yes
FDA UDI
MR Unsafe FDA UDI
LIFEPAK 1000 LiMnO2 non rechargeable battery by PHYSIO-CONTROL, Inc. — Class III — 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 III | Pending data |
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Manufacturer
- Manufacturer
- PHYSIO-CONTROL, Inc.
Sources (1)
- FDA UDI 5a85008b-2904-4dde-8fed-c2de382f4e67 36 fields · synced Jun 9, 2026