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Hermesh

FDA UDI

Class II (US FDA UDI)

by Herniamesh

Identity

Trade Name
HERMESH FDA UDI
Generic Name
Extra-gynaecological surgical mesh, synthetic polymer, non-bioabsorbable FDA UDI
Device Name
Hermesh 3 cm 6x11 is a rectangular macroporous mesh knitted with Polypropylene monofilament, indicated for both open and laparoscopic hernia repair FDA UDI
Model / Reference
H30611 FDA UDI
Description
Hermesh 3 cm 6x11 is a rectangular macroporous mesh knitted with Polypropylene monofilament, indicated for both open and laparoscopic hernia repair FDA UDI

Identifiers

Primary DI / UDI-DI
58032919890356 FDA UDI
FDA Product Code
FTL FDA UDI
GMDN Term
Extra-gynaecological surgical mesh, synthetic polymer, non-bioabsorbable 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

Yes

FDA UDI

Category: Extra-gynaecological surgical mesh, synthetic polymer, non-bioabsorbable

Hermesh by Herniamesh — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Extra-gynaecological surgical mesh, synthetic polymer, non-bioabsorbable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Herniamesh

Sources (1)

  • FDA UDI 7d417a75-cf56-468a-954a-ee76f56055e9 33 fields · synced May 30, 2026