← Back to catalogue

Microflex

FDA UDI

Class I (US FDA UDI)

by Ansell Healthcare Product

Identity

Trade Name
MICROFLEX FDA UDI
Generic Name
Nitrile examination/treatment glove, non-powdered, non-antimicrobial FDA UDI
Device Name
MICROFLEX Aloe Sense Pink L (8.5-9.0), Aloe & Chamomile Coated Nitrile Powder-Free Examination Glove FDA UDI
Model / Reference
93849090 FDA UDI
Description
MICROFLEX Aloe Sense Pink L (8.5-9.0), Aloe & Chamomile Coated Nitrile Powder-Free Examination Glove FDA UDI

Identifiers

Catalog Number
93849090 FDA UDI
Primary DI / UDI-DI
10076490432284 FDA UDI
FDA Product Code
LZC FDA UDI
QDO FDA UDI
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

Microflex by Ansell Healthcare Product — 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
Ansell Healthcare Product

Sources (1)

  • FDA UDI 88753c18-f1f3-4481-813f-f1ecc8f981ae 35 fields · synced Jun 1, 2026