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Endoch

FDA UDI

Class II (US FDA UDI)

by Endoch Inc

Identity

Trade Name
Endoch FDA UDI
Generic Name
Rigid endoscopic scissors, single-use FDA UDI
Device Name
DISPOSABLE MONOPOLAR LAPAROSCOPIC SCISSORS FDA UDI
Model / Reference
EAI-0788 FDA UDI
Description
DISPOSABLE MONOPOLAR LAPAROSCOPIC SCISSORS FDA UDI

Identifiers

Catalog Number
EAI-0788 FDA UDI
Primary DI / UDI-DI
B747EAI0788 FDA UDI
FDA Product Code
GEI FDA UDI
NWB FDA UDI
GMDN Term
Rigid endoscopic scissors, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4400 FDA UDI
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

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: Rigid endoscopic scissors, single-use

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

Similar devices

Also classified as Rigid endoscopic scissors, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Endoch Inc

Sources (1)

  • FDA UDI 396cb3e9-c7f6-4a7d-96f8-afa8cce5d72d 34 fields · synced Jun 8, 2026