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Industrial Finger Split

FDA UDI

Class I (US FDA UDI)

by Faretec, Inc.

Identity

Trade Name
Industrial Finger Split FDA UDI
Generic Name
Hand/finger splint, single-use FDA UDI
Device Name
Industrial Finger Splint Kit contains 27 assorted sizes and types of finger splints. FDA UDI
Model / Reference
Industrial Finger Splint FDA UDI
Description
Industrial Finger Splint Kit contains 27 assorted sizes and types of finger splints. FDA UDI

Identifiers

Catalog Number
1106701 FDA UDI
Primary DI / UDI-DI
B54111067010 FDA UDI
FDA Product Code
ILH FDA UDI
GMDN Term
Hand/finger splint, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.3475 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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: Hand/finger splint, single-use

Industrial Finger Split by Faretec, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Hand/finger splint, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Faretec, Inc.

Sources (1)

  • FDA UDI e135ea68-0cfb-4055-883b-58d78ee36440 35 fields · synced May 30, 2026