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Roth Net

FDA UDI

Class II (US FDA UDI)

by US Endoscopy

Identity

Trade Name
Roth Net FDA UDI
Generic Name
Gastrointestinal/airway foreign body retrieval basket, single-use FDA UDI
Device Name
The Roth Net retriever 360 product line is intended to be used to retrieve excised polyps, tissue samples, foreign bodies and calculi during flexible and rigid endoscopy procedures. FDA UDI
Model / Reference
00711198 FDA UDI
Description
The Roth Net retriever 360 product line is intended to be used to retrieve excised polyps, tissue samples, foreign bodies and calculi during flexible and rigid endoscopy procedures. FDA UDI

Identifiers

Catalog Number
00711198 FDA UDI
Primary DI / UDI-DI
00816765013649 FDA UDI
FDA Product Code
FDI FDA UDI
GCJ FDA UDI
GMDN Term
Gastrointestinal/airway foreign body retrieval basket, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.4300 FDA UDI
876.1500 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

Yes

FDA UDI

Dimensions & Sizes

Size
Width — 3 Centimeter FDA UDI
Length — 230 Centimeter FDA UDI
Outer Diameter — 2.5 Millimeter FDA UDI

Roth Net by US Endoscopy — 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
US Endoscopy

Sources (1)

  • FDA UDI be58a85a-7fa2-4e4f-beb1-cbef93ffdce3 38 fields · synced May 31, 2026