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Moray

FDA UDI

Class I (US FDA UDI)

by US Endoscopy

Identity

Trade Name
Moray FDA UDI
Generic Name
Flexible endoscopic biopsy forceps, single-use FDA UDI
Device Name
The Moray micro forceps is designed to enhance sampling from lesions that can occur within and outside of the gastrointestinal tract. FDA UDI
Model / Reference
00711889 FDA UDI
Description
The Moray micro forceps is designed to enhance sampling from lesions that can occur within and outside of the gastrointestinal tract. FDA UDI

Identifiers

Catalog Number
00711889 FDA UDI
Primary DI / UDI-DI
00724995184094 FDA UDI
FDA Product Code
FCL FDA UDI
GMDN Term
Flexible endoscopic biopsy forceps, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
876.1075 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: Flexible endoscopic biopsy forceps, single-use

Moray by US Endoscopy — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Flexible endoscopic biopsy forceps, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
US Endoscopy

Sources (1)

  • FDA UDI 7adb8db4-6818-4ffd-9bee-0c0ba7c0ec28 35 fields · synced May 30, 2026