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Intrafix

FDA UDI

Class I (US FDA UDI)

by DePuy Mitek, Inc.

Identity

Trade Name
INTRAFIX FDA UDI
Generic Name
Orthopaedic inorganic implant inserter/extractor, reusable FDA UDI
Device Name
Femoral INTRAFIX Sheath Trial 9mm - 10mm FDA UDI
Model / Reference
254667 FDA UDI
Description
Femoral INTRAFIX Sheath Trial 9mm - 10mm FDA UDI

Identifiers

Catalog Number
254667 FDA UDI
Primary DI / UDI-DI
10886705013494 FDA UDI
FDA Product Code
LXH FDA UDI
GMDN Term
Orthopaedic inorganic implant inserter/extractor, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 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

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Orthopaedic inorganic implant inserter/extractor, reusable

Intrafix by DePuy Mitek, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic inorganic implant inserter/extractor, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
DePuy Mitek, Inc.

Sources (1)

  • FDA UDI 04b67c91-a11e-4fc8-8c07-c50c5f0913ec 35 fields · synced Jun 1, 2026