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Halyard

FDA UDI

Class I (US FDA UDI)

by Ansell Healthcare Product

Identity

Trade Name
HALYARD FDA UDI
Generic Name
Polychloroprene surgical glove, non-powdered FDA UDI
Device Name
HALYARD Polyisoprene Neoprene Hybrid Size 8.5, Sterile Powder-Free Surgical Glove, Polyisoprene and Neoprene Blend FDA UDI
Model / Reference
SGL94085 FDA UDI
Description
HALYARD Polyisoprene Neoprene Hybrid Size 8.5, Sterile Powder-Free Surgical Glove, Polyisoprene and Neoprene Blend FDA UDI

Identifiers

Catalog Number
SGL94085 FDA UDI
Primary DI / UDI-DI
10680651483307 FDA UDI
FDA Product Code
KGO FDA UDI
GMDN Term
Polychloroprene surgical glove, non-powdered FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4460 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-antimicrobialPolychloroprene surgical glove, non-powdered

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

Similar devices

Also classified as Polychloroprene surgical glove, non-powdered.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 16867dd6-0e09-4f98-ab88-8c538f9acecf 36 fields · synced May 30, 2026