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Mobi-C Plug & Fit US

FDA UDI

Class II (US FDA UDI)

by Zimmer Biomet

Identity

Trade Name
Mobi-C Plug & Fit US FDA UDI
Generic Name
Spinal implant trial FDA UDI
Device Name
TRIAL 15X17 H4,5 MM FDA UDI
Model / Reference
MB9032R FDA UDI
Description
TRIAL 15X17 H4,5 MM FDA UDI

Identifiers

Primary DI / UDI-DI
03662663001052 FDA UDI
FDA Product Code
QLQ FDA UDI
GMDN Term
Spinal implant trial FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.4515 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size
Depth — 15 Millimeter FDA UDI
Width — 17 Millimeter FDA UDI

Category: Spinal implant trial

Mobi-C Plug & Fit US by Zimmer Biomet — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Spinal implant trial.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Zimmer Biomet

Sources (1)

  • FDA UDI e7923c5d-e081-4236-bbae-c4045d3646a8 35 fields · synced May 30, 2026