Consulting Wallah › Device Explorer › Endoscopy & surgical instruments › Polypectomy endoscopic ligator, single-use
Device Explorer · FDA GUDID · GMDN 38719

Polypectomy endoscopic ligator, single-use

A device used in combination with a compatible flexible endoscope for the deployment of a ligature loop (a self-locking device made of, e.g., a polymer in the form of a thin band) that is typically applied to large colorectal or pedunculated polyps in the gast

US‑registered devices52in commercial distribution
Companies4labelers on GUDID
Single‑use100%of device records
Sterile100%labelled sterile
Prescription4%Rx‑only share
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Share of device records

Beijing Zksk Technology Co.,Ltd3669%
Leo Medical Co., Ltd.1223%
Olympus Medical Systems Corp.24%
Bioseal24%

Top labelers

CompanyDevicesShare
Beijing Zksk Technology Co.,Ltd3669%
Leo Medical Co., Ltd.1223%
Olympus Medical Systems Corp.24%
Bioseal24%

Company = labeler of record on GUDID. 4 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

ZKSKLigation DeviceSINGLE USE LIGATING DEVICEBioseal Inc.

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

FDA product codes

CodeNameDevices
MNDLigator, Esophageal50
FHNLigator, Hemorrhoidal12
FDISnare, Flexible1
FHNLigator, hemorrhoidal1
ECIBAND, ELASTIC, ORTHODONTIC1

GMDN & GCC registration

  • GMDN code 38719 · non‑implantable
  • Single‑use 100% · sterile 100% · Rx‑only 4% · 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 polypectomy endoscopic ligator, single-use 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 "Polypectomy endoscopic ligator, single-use", from 4 companies. The largest labeler is Beijing Zksk Technology Co.,Ltd with 69% of records.

Which FDA product codes apply?

MND (Ligator, Esophageal), FHN (Ligator, Hemorrhoidal), FDI (Snare, Flexible), FHN (Ligator, hemorrhoidal)

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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