Identity
- Trade Name
- Spencer FDA UDI
- Generic Name
- Spine board FDA UDI
- Model / Reference
- ST02035L ROCK-STRAPS – IMMOBILIZATION BELTS ADULT BACKBOARD FDA UDI
Identifiers
- Primary DI / UDI-DI
- 08057711237180 FDA UDI
- FDA Product Code
- NZD FDA UDI
- GMDN Term
- Spine board FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 880.6900 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
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
MR Unsafe FDA UDI
Category: Spine board
Spencer by Spencer Italia Srl — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Spine board.
- EM — Allied Medical LLC · Class I
- RHINO RESCUE — Wuxi Emsrun Technology Co., Ltd. · Class I
- EMSRUN — Wuxi Emsrun Technology Co., Ltd. · Class I
- WRENCH, 5mm HEX — Bradshaw Medical Inc. · Class I
- EM — Allied Medical LLC · Class I
- MORRISON MEDICAL — MORRISON MEDICAL, LTD · Class I
- MORRISON MEDICAL — MORRISON MEDICAL, LTD · Class I
- EMSRUN — Wuxi Emsrun Technology Co., Ltd. · 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 I | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Spencer Italia Srl
Sources (1)
- FDA UDI c1a34005-9a1e-4963-b286-a02a46320df7 32 fields · synced May 30, 2026