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Cold Snare

FDA UDI

Class I (US FDA UDI)

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

Identity

Trade Name
Cold Snare FDA UDI
Generic Name
Mechanical-cutting endoscopic polypectomy snare FDA UDI
Device Name
Rhombus,Diameter of Snare is 15 mm,Outer tube is PE, diameter is 7Fr,working length is 2300mm,Non-Rotation Type FDA UDI
Model / Reference
CS3-11523230 FDA UDI
Description
Rhombus,Diameter of Snare is 15 mm,Outer tube is PE, diameter is 7Fr,working length is 2300mm,Non-Rotation Type FDA UDI

Identifiers

Primary DI / UDI-DI
06932503550024 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

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 1f3adca1-b20e-4866-a02c-1b94c1750bbe 35 fields · synced Jun 8, 2026