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AmbiCanner

FDA UDI

Class I (US FDA UDI)

by Summit Glove Inc.

Identity

Trade Name
AmbiCanner FDA UDI
Generic Name
Hevea-latex examination/treatment glove, non-powdered, non-antimicrobial FDA UDI
Device Name
12mil, 12" in length, Latex, Examination Grade, Unlined, Ambidextrous, Fishscale, Beaded Cuff, Amber Color, Size Medium FDA UDI
Model / Reference
470-8-AM FDA UDI
Description
12mil, 12" in length, Latex, Examination Grade, Unlined, Ambidextrous, Fishscale, Beaded Cuff, Amber Color, Size Medium FDA UDI

Identifiers

Primary DI / UDI-DI
00854947005921 FDA UDI
FDA Product Code
LYY FDA UDI
GMDN Term
Hevea-latex examination/treatment glove, non-powdered, non-antimicrobial 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

Yes

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Hevea-latex examination/treatment glove, non-powdered, non-antimicrobial

AmbiCanner by Summit Glove Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Hevea-latex examination/treatment glove, non-powdered, non-antimicrobial.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Summit Glove Inc.

Sources (1)

  • FDA UDI d698736d-351e-48a0-bcad-d3cf2f4560eb 34 fields · synced May 30, 2026