← Back to catalogue

Hertra

FDA UDI

Class II (US FDA UDI)

by Herniamesh

Identity

Trade Name
HERTRA FDA UDI
Generic Name
Extra-gynaecological surgical mesh, synthetic polymer, non-bioabsorbable FDA UDI
Device Name
Hertra 9A 5x11 cm is a macroporous preshaped mesh without keyhole opening, indicated for the treatment of inguinal hernia defects with open technique. FDA UDI
Model / Reference
HTR9A511 FDA UDI
Description
Hertra 9A 5x11 cm is a macroporous preshaped mesh without keyhole opening, indicated for the treatment of inguinal hernia defects with open technique. FDA UDI

Identifiers

Primary DI / UDI-DI
58032919891698 FDA UDI
510(k) Number
K973955 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

Hertra 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.

Cleared under the same submission

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
Herniamesh

Sources (1)

  • FDA UDI 5e3576e5-c2a7-4b8e-bed5-9a5fc7c3ba35 34 fields · synced Jun 8, 2026