Identity
- Trade Name
- Sprint 200 FDA UDI
- Generic Name
- Patient transfer system, manual FDA UDI
- Device Name
- The sprint stretcher transport bed. FDA UDI
- Model / Reference
- 1ES200-7 FDA UDI
- Description
- The sprint stretcher transport bed. FDA UDI
Identifiers
- Primary DI / UDI-DI
- 08592654358467 FDA UDI
- FDA Product Code
- FPO FDA UDI
- GMDN Term
- Patient transfer system, manual 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
Yes
FDA UDI
Category: Patient transfer system, manual
Sprint 200 by L I N E T spol. s r.o. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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- BRIDGE HEALTHCARE — Caremed Supply, 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
- L I N E T spol. s r.o.
Sources (1)
- FDA UDI ac83ca6e-0888-44b2-bdb0-5d955be6c8e9 33 fields · synced May 30, 2026