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Endoch

FDA UDI

Class I (US FDA UDI)

by Endoch Inc

Identity

Trade Name
Endoch FDA UDI
Generic Name
Rigid endoscopic scissors, single-use FDA UDI
Device Name
DISPOSABLE LAPAROSCOPIC BABY-METZENBAUM SCISSORS, CURVED FDA UDI
Model / Reference
EAI-0785 FDA UDI
Description
DISPOSABLE LAPAROSCOPIC BABY-METZENBAUM SCISSORS, CURVED FDA UDI

Identifiers

Catalog Number
EAI-0785 FDA UDI
Primary DI / UDI-DI
EAI0785 FDA UDI
510(k) Number
K171825 FDA UDI
FDA Product Code
JOK FDA UDI
GEI FDA UDI
GMDN Term
Rigid endoscopic scissors, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6820 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

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 I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Rigid endoscopic scissors, single-use.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Endoch Inc

Sources (1)

  • FDA UDI 4d6522cc-58b9-49e7-bfb3-0a9aad0614c5 35 fields · synced May 30, 2026