Medpor

FDA UDI

Class II (US FDA UDI)

by Stryker Leibinger

Identity

Trade Name: MEDPOR FDA UDI
Generic Name: Surgical implant template, reusable FDA UDI
Device Name: Chin Sizer Set Con Two-Pc (Sil Non-Ster) FDA UDI
Model / Reference: 85001 FDA UDI
Description: Chin Sizer Set Con Two-Pc (Sil Non-Ster) FDA UDI

Identifiers

Catalog Number: 85001 FDA UDI
Primary DI / UDI-DI: 07613252085225 FDA UDI
FDA Product Code: HQN FDA UDI
GMDN Term: Surgical implant template, reusable FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 886.3130 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Surgical implant template, reusable

Medpor by Stryker Leibinger — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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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 Leibinger

Sources (1)

FDA UDI 027a0202-7a3e-4c8d-854a-32a0f700f9d8 34 fields · synced May 30, 2026