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Menix

FDA UDI

Class I (US FDA UDI)

by S.b.m

Identity

Trade Name
MENIX FDA UDI
Generic Name
Suturing unit, reusable FDA UDI
Device Name
MENIX Knot pusher to be used with MENIX and MENIX DUO devices in meniscal repair. FDA UDI
Model / Reference
MENIX Knot pusher FDA UDI
Description
MENIX Knot pusher to be used with MENIX and MENIX DUO devices in meniscal repair. FDA UDI

Identifiers

Catalog Number
MEN9000400 FDA UDI
Primary DI / UDI-DI
03760304680748 FDA UDI
FDA Product Code
LXH FDA UDI
GMDN Term
Suturing unit, 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

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Suturing unit, reusable

Menix by S.b.m — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Suturing unit, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
S.b.m

Sources (1)

  • FDA UDI 47f27997-c59d-48ad-9f10-9052efa5aaa6 34 fields · synced May 30, 2026