Hoffmann

FDA UDI

Class II (US FDA UDI)

by Stryker Corp.

Identity

Trade Name: HOFFMANN FDA UDI
Generic Name: External orthopaedic fixation system, reusable FDA UDI
Device Name: Connecting Rod FDA UDI
Model / Reference: 5029-8-150 FDA UDI
Description: Connecting Rod FDA UDI

Identifiers

Catalog Number: 5029-8-150 FDA UDI
Primary DI / UDI-DI: 07613327079272 FDA UDI
FDA Product Code: LXT FDA UDI
JEC FDA UDI
KTT FDA UDI
GMDN Term: External orthopaedic fixation system, reusable FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 888.3030 FDA UDI
888.3040 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size: Length — 150.0 Millimeter FDA UDI

Category: External orthopaedic fixation system, reusable

Hoffmann by Stryker Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as External orthopaedic fixation system, reusable.

ADVANCED LIMB RECONSTRUCTION SYSTEM — Orthofix, Inc. · Class II
PAEDIATRIC LIMB RECONSTRUCTION SYSTEM — Orthofix, Inc. · Class II
Integra® External Fixation System — Ascension Orthopedics, Inc. · Class II
PAEDIATRIC LIMB RECONSTRUCTION SYSTEM — Orthofix, Inc. · Class II
TransFx™ — Zimmer, Inc. · Class I
SIDEKICK — WRIGHT MEDICAL TECHNOLOGY, INC. · Class II
SIDEKICK — WRIGHT MEDICAL TECHNOLOGY, INC. · Class II
SHEFFIELD RING FIXATOR — Orthofix, Inc. · Class II

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Stryker Corp.

Sources (1)

FDA UDI 69311667-0b3e-4fac-a3c8-f2a03800ed38 35 fields · synced May 30, 2026