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EndoRings

FDA UDI

Class II (US FDA UDI)

by Endo-Aid, Inc.

Identity

Trade Name
EndoRings FDA UDI
Generic Name
Colonoscope distal anchoring cuff FDA UDI
Device Name
The EndoRings is intended to be attached to the distal end of the endoscope to facilitate endoscopic therapy, to be used for the following: Keeping the suitable depth of endoscope's view field. FDA UDI
Model / Reference
E103 FDA UDI
Description
The EndoRings is intended to be attached to the distal end of the endoscope to facilitate endoscopic therapy, to be used for the following: Keeping the suitable depth of endoscope's view field. FDA UDI

Identifiers

Primary DI / UDI-DI
07290016767032 FDA UDI
FDA Product Code
FED FDA UDI
GMDN Term
Colonoscope distal anchoring cuff FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1500 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

Dimensions & Sizes

Size
Height — 24 Millimeter FDA UDI

Category: Colonoscope distal anchoring cuff

EndoRings by Endo-Aid, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Colonoscope distal anchoring cuff.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Endo-Aid, Inc.

Sources (1)

  • FDA UDI 799ad9c4-3359-45b6-b89b-6d599732b14d 34 fields · synced May 30, 2026