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Halyard

FDA UDI

Class I (US FDA UDI)

by Ansell

Identity

Trade Name
HALYARD FDA UDI
Generic Name
Polyisoprene surgical glove, non-powdered, non-antimicrobial FDA UDI
Device Name
HALYARD SGL99075 Polyisoprene Green Size (7.5), Powder-Free Polyisoprene Surgical Glove FDA UDI
Model / Reference
SGL99075 FDA UDI
Description
HALYARD SGL99075 Polyisoprene Green Size (7.5), Powder-Free Polyisoprene Surgical Glove FDA UDI

Identifiers

Catalog Number
SGL99075 FDA UDI
Primary DI / UDI-DI
10680651190755 FDA UDI
FDA Product Code
KGO FDA UDI
LZC FDA UDI
GMDN Term
Polyisoprene surgical glove, non-powdered, non-antimicrobial FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4460 FDA UDI
880.6250 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Polyisoprene surgical glove, non-powdered, non-antimicrobial

Halyard by Ansell — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Polyisoprene surgical glove, non-powdered, non-antimicrobial.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Ansell

Sources (1)

  • FDA UDI 5e696439-76f0-4539-8007-19f4f5e90268 36 fields · synced Jun 8, 2026