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Device Explorer · FDA GUDID · GMDN 38832

Hand-held examination/treatment light

A small hand-held battery-powered light intended to beused as a personal light source to provide light for local examination, inspection, and treatment of the patient. It may be torch-like in design and can have a magnifying lens to augment the lighting effect

US‑registered devices149in commercial distribution
Companies18labelers on GUDID
Single‑use9%of device records
Sterile5%labelled sterile
Prescription13%Rx‑only share
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Share of device records

American Diagnostic Corp5235%
Bv Medical4128%
Rudolf Riester Gmbh1711%
Aspen Surgical Products, Inc.149%
Mdf Instruments Medifriend Inc.43%
Beaver-Visitec International, Inc.43%
Zhejiang Honsun Medical Technology Co., Ltd.21%
Ceek Women'S Health21%

Top labelers

CompanyDevicesShare
American Diagnostic Corp5235%
Bv Medical4128%
Rudolf Riester Gmbh1711%
Aspen Surgical Products, Inc.149%
Mdf Instruments Medifriend Inc.43%
Beaver-Visitec International, Inc.43%
Zhejiang Honsun Medical Technology Co., Ltd.21%
Ceek Women'S Health21%
Medsource International Llc21%
Dynarex Corporation21%
National Distribution & Contracting, Inc.21%
Ningbo Tealmed Emergency Products Co., Ltd.11%

Company = labeler of record on GUDID. 18 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

TealmedJeashiaNAMDF®mini-fri-pen® violett,Pack of 6 pcs. ri-pen®, violette-xam LED 2.5 V, whitee-xam LED 2.5 V, blacke-xam XL 2.5 V, whitee-xam XL 2.5 V, blackri-pen® redri-pen® blackri-pen® silverri-pen® greenri-pen® blue

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

FDA product codes

CodeNameDevices
KYTLight, Examination, Medical, Battery Powered140
FTFIlluminator, Non-Remote10
LDEStethoscope, Manual5
DXQBlood Pressure Cuff5
LRWScissors, General, Surgical5
FTYTape, Measuring, Rulers And Calipers5

GMDN & GCC registration

  • GMDN code 38832 · non‑implantable
  • Single‑use 9% · sterile 5% · Rx‑only 13% · OTC 37%
  • 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 hand-held examination/treatment light products are registered in the US?

149 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Hand-held examination/treatment light", from 18 companies. The largest labeler is American Diagnostic Corp with 35% of records.

Which FDA product codes apply?

KYT (Light, Examination, Medical, Battery Powered), FTF (Illuminator, Non-Remote), LDE (Stethoscope, Manual), DXQ (Blood Pressure Cuff)

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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