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Disposable Polypectomy Cold Snare

FDA UDI

Class I (US FDA UDI)

by Yangzhou Fartley Medical Instrument Technology Co., Ltd.

Identity

Trade Name
Disposable Polypectomy Cold Snare FDA UDI
Generic Name
Mechanical-cutting endoscopic polypectomy snare FDA UDI
Model / Reference
FTL-PSC-24-230-25-10-R FDA UDI

Identifiers

Primary DI / UDI-DI
06970900855878 FDA UDI
FDA Product Code
FGX FDA UDI
GMDN Term
Mechanical-cutting endoscopic polypectomy snare 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

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

Category: Mechanical-cutting endoscopic polypectomy snare

Disposable Polypectomy Cold Snare by Yangzhou Fartley Medical Instrument Technology Co., Ltd. — Class I — FDA UDI — listed in FDA GUDID

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 b07b8647-f594-41a8-b294-79e0aca62612 32 fields · synced May 30, 2026