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Prodisc C Vivo

FDA UDI

Class III (US FDA UDI)

by Centinel Spine, LLC

Identity

Trade Name
Prodisc C Vivo FDA UDI
Generic Name
Cervical total intervertebral disc prosthesis, modular FDA UDI
Device Name
Prodisc C Vivo, Medium, 6mm FDA UDI
Model / Reference
PDVM6 FDA UDI
Description
Prodisc C Vivo, Medium, 6mm FDA UDI

Identifiers

Primary DI / UDI-DI
00843193113689 FDA UDI
PMA Number
P070001 FDA UDI
FDA Product Code
MJO FDA UDI
GMDN Term
Cervical total intervertebral disc prosthesis, modular FDA UDI

Classification

Device Class
Class III FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Conditional FDA UDI

Category: Cervical total intervertebral disc prosthesis, modular

Prodisc C Vivo by Centinel Spine, LLC — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Cervical total intervertebral disc prosthesis, modular.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Centinel Spine, LLC

Sources (1)

  • FDA UDI e7336941-a5a4-449c-9618-0090e46a1fed 34 fields · synced Jun 6, 2026