Wiggins Medical

FDA UDI

Class I (US FDA UDI)

by Ebner Medical Llc

Identity

Trade Name: Wiggins Medical FDA UDI
Generic Name: Craniofacial rongeur, reusable FDA UDI
Device Name: Black Caspar-style IVD Rongeur w/teeth, 3mm down, 9" FDA UDI
Model / Reference: 52-106-30/23B FDA UDI
Description: Black Caspar-style IVD Rongeur w/teeth, 3mm down, 9" FDA UDI

Identifiers

Catalog Number: 52-106-30/23B FDA UDI
Primary DI / UDI-DI: 00840217904384 FDA UDI
FDA Product Code: HTX FDA UDI
GMDN Term: Craniofacial rongeur, 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

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

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size: Length — 9 Inch FDA UDI
Width — 3 Millimeter FDA UDI

Category: Craniofacial rongeur, reusable

Wiggins Medical by Ebner Medical Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Also classified as Craniofacial rongeur, reusable.

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Novo Surgical Inc. — NOVO SURGICAL, INC. · Class I
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Novo Surgical Inc. — NOVO SURGICAL, INC. · Class I
BEAR — Bear-Ent, LLC · Class I
Integra® Miltex® — Integra LifeSciences Production Corporation · 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: Ebner Medical Llc

Sources (1)

FDA UDI 4987364e-2007-4c33-89e2-4489a1744925 36 fields · synced May 30, 2026