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Disposable Polyp Snare

FDA UDI

Class II (US FDA UDI)

by Jiangsu Vedkang Medical Science and Technology Co., Ltd.

Identity

Trade Name
Disposable Polyp Snare FDA UDI
Generic Name
Endoscopic electrosurgical handpiece/electrode, monopolar, single-use FDA UDI
Model / Reference
VDK-SD-23-230-10-A1 FDA UDI

Identifiers

Primary DI / UDI-DI
06970057575278 FDA UDI
510(k) Number
K220089 FDA UDI
FDA Product Code
FDI FDA UDI
GMDN Term
Endoscopic electrosurgical handpiece/electrode, monopolar, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.4300 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Endoscopic electrosurgical handpiece/electrode, monopolar, single-use

Disposable Polyp Snare by Jiangsu Vedkang Medical Science and Technology Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Endoscopic electrosurgical handpiece/electrode, monopolar, single-use.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 1c6e78a2-865f-4292-be08-152333afc587 33 fields · synced May 30, 2026