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Tac Applicator

FDA UDI

Class I (US FDA UDI)

by Surgident

Identity

Trade Name
Tac Applicator FDA UDI
Generic Name
Bone tack inserter, basic FDA UDI
Model / Reference
TA-01 FDA UDI

Identifiers

Primary DI / UDI-DI
08800041053469 FDA UDI
FDA Product Code
ECT FDA UDI
GMDN Term
Bone tack inserter, basic FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4565 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Bone tack inserter, basic

Tac Applicator by Surgident — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bone tack inserter, basic.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Surgident

Sources (1)

  • FDA UDI 45bd10b1-152b-4d85-adb7-560fa2ff3a8b 32 fields · synced Jun 8, 2026