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Echelon Flex Endopath

FDA UDI

Class II (US FDA UDI)

by Ethicon Endo-Surgery, Inc.

Identity

Trade Name
ECHELON FLEX ENDOPATH FDA UDI
Generic Name
Endoscopic manual linear cutting stapler, single-use FDA UDI
Device Name
ECHELON Flex 60 Articulating Endoscopic Linear Cutter (No Cartridge) FDA UDI
Model / Reference
EC60A FDA UDI
Description
ECHELON Flex 60 Articulating Endoscopic Linear Cutter (No Cartridge) FDA UDI

Identifiers

Catalog Number
EC60A FDA UDI
Primary DI / UDI-DI
10705036001706 FDA UDI
FDA Product Code
GDW FDA UDI
GMDN Term
Endoscopic manual linear cutting stapler, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4750 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Endoscopic manual linear cutting stapler, single-use

Echelon Flex Endopath by Ethicon Endo-Surgery, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Endoscopic manual linear cutting stapler, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 4f4d5967-fbed-4dd1-b226-65272e99d090 35 fields · synced Jun 1, 2026