Consulting Wallah › Device Explorer › Gloves & PPE › Polyisoprene surgical glove, non-powdered, antimic
Device Explorer · FDA GUDID · GMDN 59023

Polyisoprene surgical glove, non-powdered, antimicrobial

A device made of polyisoprene intended as a protective barrier when worn on the hands of healthcare providers at the surgical site; it includes an antimicrobial or antiviral agent/properties to reduce viable-microbe exposure in case of sharp penetration and it

US‑registered devices52in commercial distribution
Companies3labelers on GUDID
Single‑use100%of device records
Sterile100%labelled sterile
Prescription0%Rx‑only share
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Share of device records

Prestige Ameritech, Ltd.3160%
Shanghai Motex Healthcare Co.,Ltd.1325%
Guilin Hbm Health Protections, Inc.815%

Top labelers

CompanyDevicesShare
Prestige Ameritech, Ltd.3160%
Shanghai Motex Healthcare Co.,Ltd.1325%
Guilin Hbm Health Protections, Inc.815%

Company = labeler of record on GUDID. 3 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

DextersMocareHealthPremierPro Surgeons Glove

Sample of brand names as labelled; no endorsement. Ask us for the full list with company, model and UDI.

FDA product codes

CodeNameDevices
KGOSurgeon'S Gloves52

GMDN & GCC registration

  • GMDN code 59023 · non‑implantable
  • Single‑use 100% · sterile 100% · Rx‑only 0% · OTC 6%
  • UAE: MOHAP / DoH medical device registration and an authorised representative are required; Saudi: SFDA MDMA. We check status on request.

Size attributes recorded

Length (Inch) · 8

Use these as the dimensions to specify in a tender line.

How many polyisoprene surgical glove, non-powdered, antimicrobial products are registered in the US?

52 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Polyisoprene surgical glove, non-powdered, antimicrobial", from 3 companies. The largest labeler is Prestige Ameritech, Ltd. with 60% of records.

Which FDA product codes apply?

KGO (Surgeon'S Gloves)

Is this the same as UAE/GCC registration?

No. GUDID is the US register. For the UAE (MOHAP/DoH) and Saudi (SFDA/MDMA) a separate registration and a local authorised representative are required; Consulting Wallah can check the status and connect you with registered suppliers.

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Source: FDA AccessGUDID (AccessGUDID full release 2 Nov 2026); counts are device records in commercial distribution grouped by GMDN preferred term; companies are labelers of record. Information only — US listing is not a registration in the UAE or GCC; verify with the regulator. © Consulting Wallah — CC BY‑NC‑ND.

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