← Back to catalogue

Basic

FDA UDI

Class I (US FDA UDI)

by Intco Medical Industries, Inc.

Identity

Trade Name
BASIC FDA UDI
Generic Name
Nitrile examination/treatment glove, non-powdered, non-antimicrobial FDA UDI
Device Name
BASIC Synguard Ultra Nitrile Exam Gloves FDA UDI
Model / Reference
NGUM10177 FDA UDI
Description
BASIC Synguard Ultra Nitrile Exam Gloves FDA UDI

Identifiers

Catalog Number
NGUM10177 FDA UDI
Primary DI / UDI-DI
B845NGUM101771 FDA UDI
FDA Product Code
LZA FDA UDI
GMDN Term
Nitrile 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

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

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: Nitrile examination/treatment glove, non-powdered, non-antimicrobial

Basic by Intco Medical Industries, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

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
Intco Medical Industries, Inc.

Sources (1)

  • FDA UDI f6b73e58-52ab-481f-afbd-3ed760b4a0ee 35 fields · synced Jun 1, 2026