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Kumar T-ANCHORS® Hernia Set

FDA UDI

Class II (US FDA UDI)

by Nashville Surgical Instruments

Identity

Trade Name
Kumar T-ANCHORS® Hernia Set FDA UDI
Generic Name
Surgical mesh T fastener FDA UDI
Device Name
The Kumar T-ANCHORS® Hernia Set provides a means of Fixation of the Mesh in Laparoscopic or Open Repair of Abdominal Wall Hernia as Trans-fascial sutures, in addition to the tackers. Kumar T-ANCHORS® eliminate the need for grasping and feeding of sutures into a Suture Passer. FDA UDI
Model / Reference
TA-008 FDA UDI
Description
The Kumar T-ANCHORS® Hernia Set provides a means of Fixation of the Mesh in Laparoscopic or Open Repair of Abdominal Wall Hernia as Trans-fascial sutures, in addition to the tackers. Kumar T-ANCHORS® eliminate the need for grasping and feeding of sutures into a Suture Passer. FDA UDI

Identifiers

Catalog Number
TA-008 FDA UDI
Primary DI / UDI-DI
B361TA0080 FDA UDI
510(k) Number
K081366 FDA UDI
FDA Product Code
GDW FDA UDI
GAR FDA UDI
GMDN Term
Surgical mesh T fastener FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4750 FDA UDI
878.5020 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
MRI Safety
MR Safe FDA UDI

Category: Surgical mesh T fastener

Kumar T-ANCHORS® Hernia Set by Nashville Surgical Instruments — 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

Sources (1)

  • FDA UDI 249d5644-0438-4f20-939f-208e885bbe8c 37 fields · synced May 30, 2026