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Polypectomy Snare, Oval - Medium

FDA UDI

Class II (US FDA UDI)

by Endo-Therapeutics, Inc.

Identity

Trade Name
Polypectomy Snare, Oval - Medium FDA UDI
Generic Name
Endoscopic electrosurgical handpiece/electrode, monopolar, single-use FDA UDI
Device Name
Flexible Polypectomy Snare, Medium Oval - Hot FDA UDI
Model / Reference
SGO-1622M FDA UDI
Description
Flexible Polypectomy Snare, Medium Oval - Hot FDA UDI

Identifiers

Catalog Number
SGO-1622M FDA UDI
Primary DI / UDI-DI
00816207020679 FDA UDI
FDA Product Code
KNS 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
Not 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

No

FDA UDI

Dimensions & Sizes

Size
Outer Diameter — 2.4 Millimeter FDA UDI
Length — 220 Centimeter FDA UDI

Polypectomy Snare, Oval - Medium by Endo-Therapeutics, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Endo-Therapeutics, Inc.

Sources (1)

  • FDA UDI 7365c9db-38bf-4dba-835f-0b9d118f114d 38 fields · synced Jun 1, 2026