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Halyard

FDA UDI

Class I (US FDA UDI)

by Ansell

Identity

Trade Name
HALYARD FDA UDI
Generic Name
Polychloroprene surgical glove, non-powdered FDA UDI
Device Name
HALYARD SGL85090B Neoprene Micro Bulk Size (9.0), Powder-Free Neoprene Surgical Glove FDA UDI
Model / Reference
SGL85090B FDA UDI
Description
HALYARD SGL85090B Neoprene Micro Bulk Size (9.0), Powder-Free Neoprene Surgical Glove FDA UDI

Identifiers

Catalog Number
SGL85090B FDA UDI
Primary DI / UDI-DI
00076490718350 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: Polychloroprene surgical glove, non-powdered

Halyard by Ansell — 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

Manufacturer
Ansell

Sources (1)

  • FDA UDI 22fb3b9f-234f-4a48-b4e7-1cd7e9c12f6f 36 fields · synced May 30, 2026