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Tacker

FDA UDI

Class II (US FDA UDI)

by Covidien LP

Identity

Trade Name
Tacker FDA UDI
Generic Name
Soft-tissue/mesh anchor, non-bioabsorbable FDA UDI
Device Name
Fixation Device FDA UDI
Model / Reference
OMS-TTSD30 FDA UDI
Description
Fixation Device FDA UDI

Identifiers

Primary DI / UDI-DI
10884521070493 FDA UDI
510(k) Number
K090470 FDA UDI
FDA Product Code
GDW FDA UDI
GMDN Term
Soft-tissue/mesh anchor, non-bioabsorbable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4750 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

Dimensions & Sizes

Size
Outer Diameter — 5 Millimeter FDA UDI

Category: Soft-tissue/mesh anchor, non-bioabsorbable

Tacker by Covidien LP — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Soft-tissue/mesh anchor, 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
Covidien LP

Sources (1)

  • FDA UDI 8f095b64-9282-4894-8f1d-d678990dcf6c 37 fields · synced May 29, 2026