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GORE MYCROMESH PLUS Biomaterial

FDA UDI

Class II (US FDA UDI)

by W. L. Gore & Associates, Inc

Identity

Trade Name
GORE MYCROMESH PLUS Biomaterial FDA UDI
Generic Name
Multi-purpose surgical mesh, synthetic polymer, non-bioabsorbable, antimicrobial FDA UDI
Model / Reference
1MYMP02 FDA UDI

Identifiers

Catalog Number
1MYMP02 FDA UDI
Primary DI / UDI-DI
00733132601622 FDA UDI
510(k) Number
K063435 FDA UDI
FDA Product Code
FTL FDA UDI
GMDN Term
Multi-purpose surgical mesh, synthetic polymer, non-bioabsorbable, antimicrobial FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.3300 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Height — 1 Millimeter FDA UDI
Length — 15 Centimeter FDA UDI
Width — 5 Centimeter FDA UDI

GORE MYCROMESH PLUS Biomaterial by W. L. Gore & Associates, 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

Manufacturer
W. L. Gore & Associates, Inc

Sources (1)

  • FDA UDI d75d9198-429f-43e0-9cd7-12f7bc759ff1 37 fields · synced Jun 6, 2026