Endoch

FDA UDI

Class I (US FDA UDI)

by Endoch Inc

Identity

Trade Name: Endoch FDA UDI
Generic Name: Rigid endoscopic grasping forceps, single-use FDA UDI
Device Name: DISPOSABLE LAPAROSCOPIC GRASPING FORCEPS FDA UDI
Model / Reference: EAI-0704 FDA UDI
Description: DISPOSABLE LAPAROSCOPIC GRASPING FORCEPS FDA UDI

Identifiers

Catalog Number: EAI-0704 FDA UDI
Primary DI / UDI-DI: EAI0704 FDA UDI
FDA Product Code: GEN FDA UDI
GEI FDA UDI
GMDN Term: Rigid endoscopic grasping forceps, single-use FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 878.4800 FDA UDI
878.4400 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Rigid endoscopic grasping forceps, single-use

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

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Endoch Inc

Sources (1)

FDA UDI f2269101-3a2c-489b-9115-c18b97be5e32 34 fields · synced May 30, 2026