← Back to catalogue

Spencer

FDA UDI

Class I (US FDA UDI)

by Spencer Italia Srl

Identity

Trade Name
Spencer FDA UDI
Generic Name
Spine board FDA UDI
Model / Reference
ST02010B ROCK PIN SPINE BOARD YELLOW W/PINS FDA UDI

Identifiers

Primary DI / UDI-DI
08057711231065 FDA UDI
FDA Product Code
FPP 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
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.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Spencer Italia Srl

Sources (1)

  • FDA UDI 417f3d29-8c03-4dde-a9b1-2c6c941562ce 32 fields · synced May 30, 2026