Lsss

FDA UDI

Class I (US FDA UDI)

by Lockdown Medical Ltd

Identity

Trade Name: LSSS FDA UDI
Generic Name: Surgical depth gauge, reusable FDA UDI
Device Name: DEPTH GAUGE INNER BODY WITH BALL & SPRING. THIS INNER TUBE HAS MARKINGS ON IT. IT SITS INSIDE THE "DEPTH GAUGE OUTER BODY TUBE - RM06008 (DI NO# 05060433906)". THIS CREATES THE FINAL INSTRUMENT IN626/1 - "DEPTH GAUGE ASSEMBLY - AS01069" FDA UDI
Model / Reference: RM06009 FDA UDI
Description: DEPTH GAUGE INNER BODY WITH BALL & SPRING. THIS INNER TUBE HAS MARKINGS ON IT. IT SITS INSIDE THE "DEPTH GAUGE OUTER BODY TUBE - RM06008 (DI NO# 05060433906)". THIS CREATES THE FINAL INSTRUMENT IN626/1 - "DEPTH GAUGE ASSEMBLY - AS01069" FDA UDI

Identifiers

Catalog Number: RM06009 FDA UDI
Primary DI / UDI-DI: 05060433600913 FDA UDI
FDA Product Code: MDM FDA UDI
HTJ FDA UDI
EIL FDA UDI
GMDN Term: Surgical depth gauge, reusable FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 878.4800 FDA UDI
888.4300 FDA UDI
872.4565 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

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

FDA UDI

Category: Surgical depth gauge, reusable

Lsss by Lockdown Medical Ltd — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Summa Orthopaedics System Surgical Instrument — Jeil Medical Corporation · Class I
Trigen — Smith & Nephew, Inc. · Class I
HOOK TIP DEPTH GAUGE CLAVICLE SYSTEM — ADVANCED ORTHOPAEDIC SOLUTIONS, INC. · Class I
MSI Precision Specialty Instruments — Med Saver, Inc. · Class I
Summa Orthopaedics System Surgical Instrument — Jeil Medical 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: Lockdown Medical Ltd

Sources (1)

FDA UDI 1944352d-604c-4c4e-af00-649aa01a2607 34 fields · synced Jun 8, 2026