Champion

FDA UDI

Class I (US FDA UDI)

by Stryker Corp.

Identity

Trade Name: CHAMPION FDA UDI
Generic Name: Endoscopic surgical probe FDA UDI
Device Name: Blunt-Nose Punch, Up FDA UDI
Model / Reference: 0242100013 FDA UDI
Description: Blunt-Nose Punch, Up FDA UDI

Identifiers

Catalog Number: 0242100013 FDA UDI
Primary DI / UDI-DI: 07613327056419 FDA UDI
FDA Product Code: NBH FDA UDI
GMDN Term: Endoscopic surgical probe FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 888.1100 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

FDA UDI

Manufacturing Date

FDA UDI

Dimensions & Sizes

Size: Outer Diameter — 2.7 Millimeter FDA UDI

Category: Endoscopic surgical probe

Champion by Stryker Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Lightning — RESPONSIVE ORTHOPEDICS LLC · Class I
Rasp Probe — Biomet Orthopedics, Inc. · Class I
Lightning — RESPONSIVE ORTHOPEDICS LLC · Class I

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 I	Pending data

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Manufacturer

Manufacturer: Stryker Corp.

Sources (1)

FDA UDI 34339e03-77c7-4d8d-a36d-4abc980e1839 36 fields · synced May 29, 2026