Consulting Wallah › Device Explorer › Other devices › Radiation shielding blanket
Device Explorer · FDA GUDID · GMDN 38357

Radiation shielding blanket

A personal protective device intended to shield selected body parts of a patient, or others, from unnecessary exposure to radiation during diagnostic or therapeutic medical or dental procedures. Radiation protection blankets used in diagnostic x-ray and nuclea

US‑registered devices55in commercial distribution
Companies2labelers on GUDID
Single‑use89%of device records
Sterile82%labelled sterile
Prescription11%Rx‑only share
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Share of device records

Worldwide Innovations & Technologies, Inc.4989%
S.I.T. Sordina Iort Technologies Spa611%

Top labelers

CompanyDevicesShare
Worldwide Innovations & Technologies, Inc.4989%
S.I.T. Sordina Iort Technologies Spa611%

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

Brand names on the register (sample)

RADPADABSORBER SHIELD

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

FDA product codes

CodeNameDevices
KPYShield, protective, personnel49
IYEAccelerator, Linear, Medical6

GMDN & GCC registration

  • GMDN code 38357 · non‑implantable
  • Single‑use 89% · sterile 82% · Rx‑only 11% · 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

Circumference (Millimeter) · 6

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

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

55 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Radiation shielding blanket", from 2 companies. The largest labeler is Worldwide Innovations & Technologies, Inc. with 89% of records.

Which FDA product codes apply?

KPY (Shield, protective, personnel), IYE (Accelerator, Linear, Medical)

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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