Identity
- Trade Name
- Life Support Products (LSP) FDA UDI
- Generic Name
- Cardiopulmonary resuscitation kit, reusable FDA UDI
- Device Name
- Resuscitator, Portable Red. FDA UDI
- Model / Reference
- L175-140R FDA UDI
- Description
- Resuscitator, Portable Red. FDA UDI
Identifiers
- Catalog Number
- L175-140R FDA UDI
- Primary DI / UDI-DI
- 00026072000632 FDA UDI
- FDA Product Code
- BZD FDA UDI
- GMDN Term
- Cardiopulmonary resuscitation kit, reusable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 868.5905 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
Yes
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
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Cardiopulmonary resuscitation kit, reusable
Life Support Products (LSP) by Allied Medical LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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- Emergency Medical Products — EMERGENCY MEDICAL PRODUCTS, INC. · Class I
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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 II | Pending data |
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Manufacturer
- Manufacturer
- Allied Medical LLC
Sources (1)
- FDA UDI c975d637-dce0-48ee-9d0b-b657f1971ec4 34 fields · synced May 31, 2026