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ValuTrus

FDA UDI

Class II (US FDA UDI)

by Ethicon Endo-Surgery, Inc.

Identity

Trade Name
ValuTrus FDA UDI
Generic Name
Open-surgery manual linear cutting stapler, reusable FDA UDI
Device Name
ValuTrus Reusable Linear Stapler Handle, Reusable FDA UDI
Model / Reference
ADLH FDA UDI
Description
ValuTrus Reusable Linear Stapler Handle, Reusable FDA UDI

Identifiers

Catalog Number
ADLH FDA UDI
Primary DI / UDI-DI
20705036013980 FDA UDI
FDA Product Code
GDW FDA UDI
GMDN Term
Open-surgery manual linear cutting stapler, reusable 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

No

FDA UDI

Single Use

No

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

ValuTrus 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 62aa3de0-6f66-4bfb-a16a-551c454114ee 36 fields · synced May 30, 2026