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TIII Traction Splint

FDA UDI

Class I (US FDA UDI)

by Faretec, Inc.

Identity

Trade Name
TIII Traction Splint FDA UDI
Generic Name
First aid limb splint, non-mouldable, reusable FDA UDI
Device Name
TIII Leg traction splint with molded ratchet, Pediatric FDA UDI
Model / Reference
Pediatric/molded FDA UDI
Description
TIII Leg traction splint with molded ratchet, Pediatric FDA UDI

Identifiers

Catalog Number
1123512 FDA UDI
Primary DI / UDI-DI
B54111235120 FDA UDI
FDA Product Code
HSP FDA UDI
GMDN Term
First aid limb splint, non-mouldable, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.5890 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

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

TIII Traction Splint by Faretec, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Faretec, Inc.

Sources (1)

  • FDA UDI a1f20fde-806c-47d8-b90a-94bd231498af 35 fields · synced May 30, 2026