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sunnycare

FDA UDI

Class I (US FDA UDI)

by Agio Group Inc.

Identity

Trade Name
sunnycare FDA UDI
Generic Name
Vinyl examination/treatment glove, non-powdered FDA UDI
Device Name
SUNNYCARE brand vinyl examination gloves powder free clear medium size 100pcs/box 10 boxes/case FDA UDI
Model / Reference
7602 FDA UDI
Description
SUNNYCARE brand vinyl examination gloves powder free clear medium size 100pcs/box 10 boxes/case FDA UDI

Identifiers

Catalog Number
7602 FDA UDI
Primary DI / UDI-DI
10850044355836 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Vinyl examination/treatment glove, non-powdered

sunnycare by Agio Group 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

Manufacturer
Agio Group Inc.

Sources (1)

  • FDA UDI 4d075a29-a722-4bf2-ac07-7fa0d9adeb14 34 fields · synced May 30, 2026