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EnTrap(TM) Polyp Retrieval Snare Net

FDA UDI

Class I (US FDA UDI)

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

Identity

Trade Name
EnTrap(TM) Polyp Retrieval Snare Net FDA UDI
Generic Name
Endoscope working-channel valve, single-use FDA UDI
Device Name
White color handle, Oval, 1*7 wire,Diameteris 30 mm,outer diameter is 2.54mm,working length is 2300mm,working channel2.8mm FDA UDI
Model / Reference
NT-E-30/23-P FDA UDI
Description
White color handle, Oval, 1*7 wire,Diameteris 30 mm,outer diameter is 2.54mm,working length is 2300mm,working channel2.8mm FDA UDI

Identifiers

Primary DI / UDI-DI
06932503554510 FDA UDI
FDA Product Code
FGX FDA UDI
GMDN Term
Endoscope working-channel valve, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
876.4730 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

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 — 2.54 Millimeter FDA UDI
Length — 230 Centimeter FDA UDI

Category: Endoscope working-channel valve, single-use

EnTrap(TM) Polyp Retrieval Snare Net by Micro-Tech (Nanjing) Co., Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Endoscope working-channel valve, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 943260b4-81d6-4400-8d8f-f08bc0e78892 35 fields · synced May 30, 2026