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Multifire VersaTack

FDA UDI

Class II (US FDA UDI)

by Covidien LP

Identity

Trade Name
Multifire VersaTack FDA UDI
Generic Name
Surgical staple loading unit, non-cutting FDA UDI
Device Name
Hernia Stapler FDA UDI
Model / Reference
174023 FDA UDI
Description
Hernia Stapler FDA UDI

Identifiers

Primary DI / UDI-DI
10884521070578 FDA UDI
510(k) Number
K912097 FDA UDI
FDA Product Code
GCJ FDA UDI
GMDN Term
Surgical staple loading unit, non-cutting FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1500 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 Conditional FDA UDI

Dimensions & Sizes

Size
Height — 4.8 Millimeter FDA UDI

Category: Surgical staple loading unit, non-cutting

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

Similar devices

Also classified as Surgical staple loading unit, non-cutting.

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 44f4a8d9-c4ea-480c-b4dd-6938e9d00aff 37 fields · synced May 30, 2026