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Tornier Perform Humeral System

FDA UDI

Class II (US FDA UDI)

by Tornier, Inc.

Identity

Trade Name
Tornier Perform Humeral System FDA UDI
Generic Name
Orthopaedic bone screw (non-sliding) FDA UDI
Device Name
Fracture Stem Screw FDA UDI
Model / Reference
PFX00124 FDA UDI
Description
Fracture Stem Screw FDA UDI

Identifiers

Catalog Number
PFX00124 FDA UDI
Primary DI / UDI-DI
00846832093434 FDA UDI
FDA Product Code
PAO FDA UDI
HSD FDA UDI
KWT FDA UDI
PHX FDA UDI
KWS FDA UDI
GMDN Term
Orthopaedic bone screw (non-sliding) FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3660 FDA UDI
888.3690 FDA UDI
888.3650 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI
MRI Safety
MR Conditional FDA UDI

Dimensions & Sizes

Size
Length — 24 Millimeter FDA UDI

Category: Orthopaedic bone screw (non-sliding)

Tornier Perform Humeral System by Tornier, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic bone screw (non-sliding).

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Tornier, Inc.

Sources (1)

  • FDA UDI c97a7361-9f75-4586-98c5-c551114136da 36 fields · synced May 31, 2026