AccessGUDID - DEVICE: EnTrap(TM) Polyp Retrieval Snare Net (06932503554510)

GUDID

Device Identifier (DI) Information

Brand Name: EnTrap(TM) Polyp Retrieval Snare Net
Version or Model: NT-E-30/23-P
Commercial Distribution Status: In Commercial Distribution
Catalog Number:
Company Name: Micro-Tech (Nanjing) Co., Ltd.

Primary DI Number: 06932503554510
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 530269083 *Terms of Use

Device Description: White color handle, Oval, 1*7 wire,Diameteris 30 mm,outer diameter is 2.54mm,working length is 2300mm,working channel2.8mm

Device Characteristics

What MRI safety information does the labeling contain?	Labeling does not contain MRI Safety Information
Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437):	No
Device labeled as "Not made with natural rubber latex":	Yes
For Single-Use:	Yes
Prescription Use (Rx):	Yes
Over the Counter (OTC):	No
Kit:	No
Combination Product:	No
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P):	No

GMDN

[?]

GMDN Term Code	GMDN Term Name	GMDN Term Definition	GMDN Term Status [?]	Implantable?
62145	Endoscope working-channel valve, single-use	A device in the form of a small attachment intended to be fitted to the working channel (including biopsy port) of an endoscope to enable access for, and/or exchange of, an endoscopic device while minimizing leakage of liquids and gasses during an endoscopic procedure. Also referred to as a seal, it may be Luer formatted and include features to allow for simultaneous irrigation/biopsy or suction via the working channel. This is a single-use device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
FGX	Snare, Non-Electrical

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
Premarket Submission Number Not Available/Not Released

Device Exempt from Premarket Submission: Yes CLOSE

Sterilization

Device Packaged as Sterile: No
Requires Sterilization Prior to Use: No

Sterilization Method [?]
No Sterilization Methods Found

Storage and Handling

[?]

Storage and Handling
No storage/handling found

Clinically Relevant Size

[?]

Size Type Text
Outer Diameter: 2.54 Millimeter
Length: 230 Centimeter

Device Record Status

Public Device Record Key: 943260b4-81d6-4400-8d8f-f08bc0e78892
Public Version Date: May 02, 2025
Public Version Number: 1
DI Record Publish Date: April 24, 2025

Alternative and Additional Identifiers Additional Identifiers

Package DI

[?]

Package DI Number	Quantity per Package	Contains DI Package	Package Status	Package Type
16932503554517	10	06932503554510	In Commercial Distribution	BOX
26932503554514	10	16932503554517	In Commercial Distribution	CASE
56932503554515	2	06932503554510	In Commercial Distribution	BOX
66932503554512	25	56932503554515	In Commercial Distribution	CASE