Spencer

FDA UDI

Class I (US FDA UDI)

by Spencer Italia Srl

Identity

Trade Name: Spencer FDA UDI
Generic Name: First aid limb splint, non-mouldable, reusable FDA UDI
Model / Reference: SR01010A DAVIS SISTEMA DI TRAZIONE ADULTO FDA UDI

Identifiers

Primary DI / UDI-DI: 08057711231492 FDA UDI
FDA Product Code: NOC FDA UDI
GMDN Term: First aid limb splint, non-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

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

MRI Safety

MR Unsafe FDA UDI

Category: First aid limb splint, non-mouldable, reusable

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

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TIII Traction Splint — FARETEC, INC. · Class I
MedSource Traction Splint — MEDSOURCE INTERNATIONAL LLC · Class I
MORRISON MEDICAL — MORRISON MEDICAL, LTD · Class I
MORRISON MEDICAL — MORRISON MEDICAL, LTD · Class I
MORRISON MEDICAL — MORRISON MEDICAL, 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

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Manufacturer

Manufacturer: Spencer Italia Srl

Sources (1)

FDA UDI e2cb72e9-65e1-4494-b4f0-27937f7e97f3 32 fields · synced Jun 8, 2026