Identity
- Trade Name
- Power-PRO FDA UDI
- Generic Name
- Ambulance stretcher docking device FDA UDI
- Model / Reference
- 6387 FDA UDI
Identifiers
- Catalog Number
- 6387-000-000 FDA UDI
- Primary DI / UDI-DI
- 07613327278057 FDA UDI
- FDA Product Code
- FPO FDA UDI
- GMDN Term
- Ambulance stretcher docking device FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.6910 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
Yes
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Ambulance stretcher docking device
Power-PRO by Stryker Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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- Load Ramp — LIFEPORT, LLC. · Class I
- PLUS — LIFEPORT, LLC. · Class I
- PLUS — LIFEPORT, LLC. · Class I
- Patient Loading Utility System (PLUS) — LIFEPORT, LLC. · Class I
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
- Stryker Corp.
Sources (1)
- FDA UDI e69f6515-f30a-4d0c-bd2c-4ec03e30a1df 33 fields · synced May 31, 2026