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Multiple Loop Polypectomy Snare

FDA UDI

Class II (US FDA UDI)

by Avanos Medical, Inc.

Identity

Trade Name
Multiple Loop Polypectomy Snare FDA UDI
Generic Name
Mechanical-cutting endoscopic polypectomy snare FDA UDI
Device Name
Polypectomy Snare FDA UDI
Model / Reference
92674 FDA UDI
Description
Polypectomy Snare FDA UDI

Identifiers

Catalog Number
60419 FDA UDI
Primary DI / UDI-DI
00350770926742 FDA UDI
FDA Product Code
FDI FDA UDI
GMDN Term
Mechanical-cutting endoscopic polypectomy snare 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: Mechanical-cutting endoscopic polypectomy snare

Multiple Loop Polypectomy Snare by Avanos Medical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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 6b13569f-5930-4727-aa9f-aae78291bb42 35 fields · synced Jun 9, 2026