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Plastalume

FDA UDI

Class I (US FDA UDI)

by Brownmed, Inc.

Identity

Trade Name
Plastalume FDA UDI
Generic Name
Hand/finger splint, reusable FDA UDI
Device Name
Strips FDA UDI
Model / Reference
10623 FDA UDI
Description
Strips FDA UDI

Identifiers

Primary DI / UDI-DI
00082161106234 FDA UDI
FDA Product Code
FYH FDA UDI
GMDN Term
Hand/finger splint, 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

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

No

FDA UDI

Category: Hand/finger splint, reusable

Plastalume by Brownmed, Inc. — 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
Brownmed, Inc.

Sources (1)

  • FDA UDI 11b6e554-e666-46bf-9bc7-1aec85cfd8de 33 fields · synced May 30, 2026