Wiggins medical

FDA UDI

Class I (US FDA UDI)

by Ebner Medical Llc

Identity

Trade Name: Wiggins medical FDA UDI
Generic Name: Suture knot pusher, reusable FDA UDI
Device Name: Bayonet Rotatable knot Pusher with 16mm length,3mm shaft FDA UDI
Model / Reference: 90-401-WM7 FDA UDI
Description: Bayonet Rotatable knot Pusher with 16mm length,3mm shaft FDA UDI

Identifiers

Primary DI / UDI-DI: 00840217909952 FDA UDI
FDA Product Code: HCF FDA UDI
GMDN Term: Suture knot pusher, reusable FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 878.4800 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

Yes

FDA UDI

Prescription Use

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

Category: Suture knot pusher, reusable

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

Similar devices

Also classified as Suture knot pusher, reusable.

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Hayden Medical — Hayden Medical Inc · Class II
PASHLEY LARYNGOSCOPE KNOT PUSHER — SONTEC INSTRUMENTS, INC. · Class I
Closed Knot Pusher — Biomet Orthopedics, Inc. · Class I
Millennium — AVALIGN TECHNOLOGIES, Inc. · Class II
MICTEC KNOT PUSHER — SONTEC INSTRUMENTS, INC. · Class II
V. Mueller — STERIS CORPORATION · Class I
Millennium — AVALIGN TECHNOLOGIES, Inc. · 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 a57eebce-b1e9-4f95-b977-c4378c6596ac 34 fields · synced May 29, 2026