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Ethicon Omnex

FDA UDI

Class III (US FDA UDI)

by Ethicon Inc.

Identity

Trade Name
ETHICON OMNEX FDA UDI
Generic Name
Skin-approximation adhesive FDA UDI
Model / Reference
4901 FDA UDI

Identifiers

Catalog Number
4901 FDA UDI
Primary DI / UDI-DI
10705031133105 FDA UDI
FDA Product Code
NBE FDA UDI
GMDN Term
Skin-approximation adhesive FDA UDI

Classification

Device Class
Class III FDA UDI
Commercial Distribution
Not 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

Ethicon Omnex by Ethicon Inc. — Class III — 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

Manufacturer
Ethicon Inc.

Sources (1)

  • FDA UDI 80eca7be-7529-4a2f-b81d-eb83d8fbd949 35 fields · synced May 31, 2026