← Back to catalogue

Endopath

FDA UDI

Class II (US FDA UDI)

by Ethicon Endo-Surgery, Inc.

Identity

Trade Name
ENDOPATH FDA UDI
Generic Name
Surgical staple loading unit, non-cutting FDA UDI
Device Name
GRAY CART RELOAD-LINEAR CUTTER FDA UDI
Model / Reference
6R45M FDA UDI
Description
GRAY CART RELOAD-LINEAR CUTTER FDA UDI

Identifiers

Catalog Number
6R45M FDA UDI
Primary DI / UDI-DI
20705036000850 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

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

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

Manufacturer

Sources (1)

  • FDA UDI aeea81f0-6fde-42a1-9860-93395e64a30e 36 fields · synced May 30, 2026