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Endopath Xcel Optiview

FDA UDI

Class II (US FDA UDI)

by Ethicon Endo-Surgery, Inc.

Identity

Trade Name
ENDOPATH XCEL OPTIVIEW FDA UDI
Generic Name
Laparoscopic access cannula, single-use FDA UDI
Device Name
Endopath Xcel with OPTIVIEW Technology Blunt Tip Trocars with Smooth Sleeves FDA UDI
Model / Reference
2H12LP FDA UDI
Description
Endopath Xcel with OPTIVIEW Technology Blunt Tip Trocars with Smooth Sleeves FDA UDI

Identifiers

Catalog Number
2H12LP FDA UDI
Primary DI / UDI-DI
10705036014256 FDA UDI
FDA Product Code
GCJ FDA UDI
GMDN Term
Laparoscopic access cannula, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1500 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: Laparoscopic access cannula, single-use

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

Similar devices

Also classified as Laparoscopic access cannula, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 7ad49721-1f82-4335-b43e-6d284c585812 35 fields · synced Jun 8, 2026