Identity
- Trade Name
- BATTERY, LI-ION, WITH IFU, LP35 FDA UDI
- Generic Name
- Portable/mobile rechargeable battery pack FDA UDI
- Device Name
- BATTERY, LI-ION, LP35 FDA UDI
- Model / Reference
- 11335 FDA UDI
- Description
- BATTERY, LI-ION, LP35 FDA UDI
Identifiers
- Catalog Number
- 11335-000001 FDA UDI
- Primary DI / UDI-DI
- 00883873790144 FDA UDI
- PMA Number
- P160026 FDA UDI
- FDA Product Code
- MKJ FDA UDI
- GMDN Term
- Portable/mobile rechargeable battery pack FDA UDI
Classification
- Device Class
- Class III FDA UDI
- Regulation Number
- 870.5310 FDA UDI
- Commercial Distribution
- 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
Category: Portable/mobile rechargeable battery pack
Battery, Li-Ion, With Ifu, Lp35 by PHYSIO-CONTROL, Inc. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Portable/mobile rechargeable battery pack.
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- ALPHA SOURCE BATTERY — ALPHA SOURCE INC. · Class III
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- R&D Batteries, Inc. — R & D BATTERIES, INC. · Class II
- R&D Batteries, Inc. — R & D BATTERIES, INC. · Class I
- R&D Batteries, Inc. — R & D BATTERIES, INC. · Class II
Cleared under the same submission
P160026 also covers:
- ASSY, CABLE, THERAPY, LP35 — PHYSIO-CONTROL, Inc.
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- LIFEPAK 1000 defibrillator — PHYSIO-CONTROL, Inc.
- LIFEPAK 1000 defibrillator — PHYSIO-CONTROL, Inc.
- LIFEPAK 1000 defibrillator — PHYSIO-CONTROL, Inc.
- LIFEPAK 1000 defibrillator — PHYSIO-CONTROL, Inc.
- LIFEPAK 1000 defibrillator — PHYSIO-CONTROL, Inc.
- LIFEPAK 1000 defibrillator — PHYSIO-CONTROL, Inc.
- LIFEPAK 15 MONITOR/DEFIBRILLATOR — PHYSIO-CONTROL, Inc.
- LIFEPAK 15 Monitor/Defibrillator — PHYSIO-CONTROL, Inc.
- LIFEPAK 15 monitor/defibrillator — PHYSIO-CONTROL, Inc.
- LIFEPAK 15 monitor/defibrillator — PHYSIO-CONTROL, Inc.
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 eca7a104-4cfb-44cf-852e-cb4166880e71 36 fields · synced Jun 9, 2026