Identity
- Trade Name
- Prime Series FDA UDI
- Generic Name
- Radiographic stretcher FDA UDI
- Model / Reference
- 1105 FDA UDI
Identifiers
- Catalog Number
- 1105-000-000XE FDA UDI
- Primary DI / UDI-DI
- 07613327278224 FDA UDI
- FDA Product Code
- FPO FDA UDI
- GMDN Term
- Radiographic stretcher 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: Radiographic stretcher
Prime Series by Stryker Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Radiographic stretcher.
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- NOA Medical Industries — Hoffmann NOA Medical Industries, LLC · Class II
- Cogent — FU SHUN HSING TECHNOLOGY CO., LTD. · Class II
- Prime Series — Stryker Corp. · Class II
- Prime Series — Stryker Corp. · Class II
- Prime Series — Stryker Corp. · Class II
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 812d933c-2fa3-4055-bab8-9e2365f2138e 34 fields · synced May 30, 2026