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gastroduodenal FTRD prOVE Cap

FDA UDI

Class I (US FDA UDI)

by Ovesco Endoscopy AG

Identity

Trade Name
gastroduodenal FTRD prOVE Cap FDA UDI
Generic Name
Endoscopic electrosurgical biopsy/resection cap trial FDA UDI
Device Name
FTRD application cap for verification of possible application of the gastroduodenal FTRD® Set and diagnostic FTRD® Set (accessability and ability to pull lesion into the cap). FDA UDI
Model / Reference
FTRD 13 FDA UDI
Description
FTRD application cap for verification of possible application of the gastroduodenal FTRD® Set and diagnostic FTRD® Set (accessability and ability to pull lesion into the cap). FDA UDI

Identifiers

Catalog Number
200.77 FDA UDI
Primary DI / UDI-DI
04260206311171 FDA UDI
FDA Product Code
FEI FDA UDI
GMDN Term
Endoscopic electrosurgical biopsy/resection cap trial FDA UDI

Classification

Device Class
Class I 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

Yes

FDA UDI

Category: Endoscopic electrosurgical biopsy/resection cap trial

gastroduodenal FTRD prOVE Cap by Ovesco Endoscopy AG — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Endoscopic electrosurgical biopsy/resection cap trial.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Ovesco Endoscopy AG

Sources (1)

  • FDA UDI 28fb62bc-f9d2-425a-9c1d-758bb5b09ddd 36 fields · synced May 31, 2026