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Better Touch

FDA UDI

Class I (US FDA UDI)

by Central Association For The Blind, Inc.

Identity

Trade Name
Better Touch FDA UDI
Generic Name
Vinyl examination/treatment glove, non-powdered FDA UDI
Model / Reference
804.4 FDA UDI

Identifiers

Primary DI / UDI-DI
00815947004352 FDA UDI
FDA Product Code
LYZ FDA UDI
GMDN Term
Vinyl examination/treatment glove, non-powdered FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6250 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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Vinyl examination/treatment glove, non-powdered

Better Touch by Central Association For The Blind, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Vinyl examination/treatment glove, non-powdered.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 1cb93b92-61cc-4eb4-b7b6-30f6adc4726f 32 fields · synced Jun 8, 2026