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Echelon Endopath

FDA UDI

Class II (US FDA UDI)

by Ethicon Endo-Surgery, Inc.

Identity

Trade Name
ECHELON ENDOPATH FDA UDI
Generic Name
Surgical staple loading unit, non-cutting FDA UDI
Device Name
Endoscopic Linear Cutter Reloads Black 4.4mm, 6 rows FDA UDI
Model / Reference
ECR60T FDA UDI
Description
Endoscopic Linear Cutter Reloads Black 4.4mm, 6 rows FDA UDI

Identifiers

Catalog Number
ECR60T FDA UDI
Primary DI / UDI-DI
20705036014369 FDA UDI
FDA Product Code
GDW FDA UDI
GMDN Term
Surgical staple loading unit, non-cutting FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4750 FDA UDI
Commercial Distribution
Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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
MRI Safety
MR Conditional FDA UDI

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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 208bccdd-5864-4f9f-8da5-9f039624d94d 36 fields · synced May 30, 2026