← Back to catalogue

Echelon

FDA UDI

Class II (US FDA UDI)

by Ethicon Endo-Surgery, Inc.

Identity

Trade Name
ECHELON FDA UDI
Generic Name
Endoscopic motorized cutting stapler, single-use FDA UDI
Device Name
ECHELON 3000 60MM COMPACT FDA UDI
Model / Reference
ECH60C FDA UDI
Description
ECHELON 3000 60MM COMPACT FDA UDI

Identifiers

Catalog Number
ECH60C FDA UDI
Primary DI / UDI-DI
10705036034971 FDA UDI
FDA Product Code
GAG FDA UDI
GMDN Term
Endoscopic motorized cutting stapler, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4740 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 motorized cutting stapler, single-use

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

Similar devices

Also classified as Endoscopic motorized cutting stapler, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Ethicon Endo-Surgery, Inc.

Sources (1)

  • FDA UDI 8786a284-94bb-4428-bd04-885da28fa140 36 fields · synced Jun 1, 2026