Consulting Wallah › Device Explorer › Gloves & PPE › Radiation shielding glove
Device Explorer · FDA GUDID · GMDN 38364

Radiation shielding glove

A personal protective device used to shield the entire hand or hands of an individual (i.e., the operator or other attending person) from unnecessary exposure to primary and scattered radiation associated with diagnostic and therapeutic medical procedures. Eac

US‑registered devices50in commercial distribution
Companies2labelers on GUDID
Single‑use100%of device records
Sterile100%labelled sterile
Prescription20%Rx‑only share
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Share of device records

Emerson & Co Srl4080%
Mundy Medical Marketing Inc1020%

Top labelers

CompanyDevicesShare
Emerson & Co Srl4080%
Mundy Medical Marketing Inc1020%

Company = labeler of record on GUDID. 2 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

Fluoro-ShieldXguardProtech Proguard

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

FDA product codes

CodeNameDevices
LZCPatient Examination Glove, Specialty38
IWPRadiographic Protective Glove12

GMDN & GCC registration

  • GMDN code 38364 · non‑implantable
  • Single‑use 100% · sterile 100% · Rx‑only 20% · OTC 0%
  • UAE: MOHAP / DoH medical device registration and an authorised representative are required; Saudi: SFDA MDMA. We check status on request.

Size attributes recorded

No structured size data on the register.

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

How many radiation shielding glove products are registered in the US?

50 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Radiation shielding glove", from 2 companies. The largest labeler is Emerson & Co Srl with 80% of records.

Which FDA product codes apply?

LZC (Patient Examination Glove, Specialty), IWP (Radiographic Protective Glove)

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.

How do I get quotes?

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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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