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Plug T2

FDA UDI

Class II (US FDA UDI)

by Herniamesh

Identity

Trade Name
PLUG T2 FDA UDI
Generic Name
Extra-gynaecological surgical mesh, synthetic polymer, non-bioabsorbable FDA UDI
Device Name
Plug T2 7 cm is a three-dimensional plug on a macroporous round base with rigid tip, indicated for the treatment of inguinal and femoral hernia defects with open technique. FDA UDI
Model / Reference
PT2/7 FDA UDI
Description
Plug T2 7 cm is a three-dimensional plug on a macroporous round base with rigid tip, indicated for the treatment of inguinal and femoral hernia defects with open technique. FDA UDI

Identifiers

Primary DI / UDI-DI
18032919891089 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

Plug T2 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

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Manufacturer

Manufacturer
Herniamesh

Sources (1)

  • FDA UDI 4d66c2bf-e7ca-4cbe-b42b-072c392e7b88 34 fields · synced May 29, 2026