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Endoch

FDA UDI

Class II (US FDA UDI)

by Endoch Inc

Identity

Trade Name
Endoch FDA UDI
Generic Name
Flexible endoscopic tissue manipulation forceps, reusable FDA UDI
Device Name
DISPOSABLE HOT BIOPSY FORCEPS, WITH SPIKE, NON-COATED FDA UDI
Model / Reference
DGF-2318A FDA UDI
Description
DISPOSABLE HOT BIOPSY FORCEPS, WITH SPIKE, NON-COATED FDA UDI

Identifiers

Catalog Number
DGF-2318A FDA UDI
Primary DI / UDI-DI
DGF23181 FDA UDI
FDA Product Code
GEI FDA UDI
GEN FDA UDI
GMDN Term
Flexible endoscopic tissue manipulation forceps, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4400 FDA UDI
878.4800 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

No

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Flexible endoscopic tissue manipulation forceps, single-useFlexible endoscopic tissue manipulation forceps, reusable

Endoch by Endoch Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Flexible endoscopic tissue manipulation forceps, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Endoch Inc

Sources (1)

  • FDA UDI 1e7c0aad-2330-429b-9381-063bdb4022d1 34 fields · synced Jun 1, 2026