Mobi-C® Plug & Fit US

FDA UDI

Class III (US FDA UDI)

by Ldr Spine USA

Identity

Trade Name: Mobi-C® Plug & Fit US FDA UDI
Generic Name: Spinal implant trial FDA UDI
Device Name: Total Cervical Disc Replacement System: Trial FDA UDI
Model / Reference: MB9033R FDA UDI
Description: Total Cervical Disc Replacement System: Trial FDA UDI

Identifiers

Primary DI / UDI-DI: 03662663001069 FDA UDI
FDA Product Code: MJO FDA UDI
GMDN Term: Spinal implant trial FDA UDI

Classification

Device Class: Class III 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

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size: Height — 5 Millimeter FDA UDI
Width — 17 Millimeter FDA UDI
Depth — 15 Millimeter FDA UDI

Category: Spinal implant trial

Mobi-C® Plug & Fit US by Ldr Spine USA — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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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 III	Pending data

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Manufacturer

Manufacturer: Ldr Spine USA

Sources (1)

FDA UDI 9f875b7d-2119-4be5-8d38-1866563a91f2 35 fields · synced May 31, 2026