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McKie Thumb Splint Pediatric

FDA UDI

Class I (US FDA UDI)

by McKie Splints, LLC

Identity

Trade Name
McKie Thumb Splint Pediatric FDA UDI
Generic Name
Hand/finger splint, reusable FDA UDI
Device Name
McKie Thumb Splint - Pediatric Size 3 - Right Hand -Black Color FDA UDI
Model / Reference
P3-R Black FDA UDI
Description
McKie Thumb Splint - Pediatric Size 3 - Right Hand -Black Color FDA UDI

Identifiers

Primary DI / UDI-DI
00810026960789 FDA UDI
FDA Product Code
ILH FDA UDI
GMDN Term
Hand/finger splint, reusable 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

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

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, reusable

McKie Thumb Splint Pediatric by McKie Splints, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Hand/finger splint, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
McKie Splints, LLC

Sources (1)

  • FDA UDI b37ea95b-9f9c-4630-b46d-807d388cf842 34 fields · synced May 30, 2026