← Back to catalogue

Artisyn

FDA UDI

Class II (US FDA UDI)

by Johnson & Johnson Medical, Inc.

Identity

Trade Name
ARTISYN FDA UDI
Generic Name
Pelvic organ prolapse surgical mesh, composite-polymer FDA UDI
Device Name
Artisyn Y-Shaped Mesh FDA UDI
Model / Reference
ARTY FDA UDI
Description
Artisyn Y-Shaped Mesh FDA UDI

Identifiers

Catalog Number
ARTY FDA UDI
Primary DI / UDI-DI
10705031202795 FDA UDI
FDA Product Code
OTO FDA UDI
GMDN Term
Pelvic organ prolapse surgical mesh, composite-polymer FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.3300 FDA UDI
Commercial Distribution
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

Category: Pelvic organ prolapse surgical mesh, composite-polymer

Artisyn by Johnson & Johnson Medical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Pelvic organ prolapse surgical mesh, composite-polymer.

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

Manufacturer
Johnson & Johnson Medical, Inc.

Sources (1)

  • FDA UDI 3ec693e1-2a41-4eb8-a1e1-9c5d1bacb84c 36 fields · synced Jun 8, 2026