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LesionHunter(TM) Rotatable Nitinol Cold Snare

FDA UDI

Class I (US FDA UDI)

by Micro-Tech (Nanjing) Co., Ltd.

Identity

Trade Name
LesionHunter(TM) Rotatable Nitinol Cold Snare FDA UDI
Generic Name
Mechanical-cutting endoscopic polypectomy snare FDA UDI
Device Name
Oval Snare loop, Rotatable, Coated spring tube, Nitinol wire Snare loop, Diameter of Snare loop is 15 mm, working length is 2300mm, the maximum outside diameter of the insertion part is 2.3mm FDA UDI
Model / Reference
CS2-21523231 FDA UDI
Description
Oval Snare loop, Rotatable, Coated spring tube, Nitinol wire Snare loop, Diameter of Snare loop is 15 mm, working length is 2300mm, the maximum outside diameter of the insertion part is 2.3mm FDA UDI

Identifiers

Primary DI / UDI-DI
06932503550062 FDA UDI
FDA Product Code
GAE FDA UDI
GMDN Term
Mechanical-cutting endoscopic polypectomy snare FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Outer Diameter — 2.3 Millimeter FDA UDI
Length — 230 Centimeter FDA UDI

Category: Mechanical-cutting endoscopic polypectomy snare

LesionHunter(TM) Rotatable Nitinol Cold Snare by Micro-Tech (Nanjing) Co., Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Mechanical-cutting endoscopic polypectomy snare.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI e0e87858-061d-464d-ba54-da7629b146cf 35 fields · synced May 30, 2026