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Spencer

FDA UDI

Class I (US FDA UDI)

by Spencer Italia Srl

Identity

Trade Name
Spencer FDA UDI
Generic Name
First aid limb splint, mouldable, reusable FDA UDI
Model / Reference
JM80006A BLUE SPLINT - STECC. RIGIDA POLSO cm 30 FDA UDI

Identifiers

Primary DI / UDI-DI
08057711230389 FDA UDI
FDA Product Code
NOC FDA UDI
GMDN Term
First aid limb splint, mouldable, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.3910 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
MRI Safety
MR Unsafe FDA UDI

Category: First aid limb splint, mouldable, reusable

Spencer by Spencer Italia Srl — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as First aid limb splint, mouldable, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Spencer Italia Srl

Sources (1)

  • FDA UDI a37d3ed4-aae2-4aa4-8e31-6f51d69d4220 32 fields · synced May 30, 2026