← Back to catalogue

Walgreens

FDA UDI

Class I (US FDA UDI)

by Walgreen Co.

Identity

Trade Name
WALGREENS FDA UDI
Generic Name
Hand/finger splint, single-use FDA UDI
Device Name
Walgreens Custom Fit MySplint Wrist Support FDA UDI
Model / Reference
875421 FDA UDI
Description
Walgreens Custom Fit MySplint Wrist Support FDA UDI

Identifiers

Primary DI / UDI-DI
00049022060029 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

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Hand/finger splint, single-use

Walgreens by Walgreen Co. — 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Walgreen Co.

Sources (1)

  • FDA UDI e7bac00e-79eb-4e42-a969-a5fdb7e059f6 34 fields · synced May 31, 2026