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Cervical Interbody 13mm x 12mm x 5mm Packaging

FDA UDI

Class II (US FDA UDI)

by Xenco Medical Llc

Identity

Trade Name
Cervical Interbody 13mm x 12mm x 5mm Packaging FDA UDI
Generic Name
Spinal fixation plate, non-bioabsorbable FDA UDI
Device Name
Cervical Interbody 13mm x 12mm x 5mm FDA UDI
Model / Reference
XM-112-1305 FDA UDI
Description
Cervical Interbody 13mm x 12mm x 5mm FDA UDI

Identifiers

Primary DI / UDI-DI
B064XM11213051 FDA UDI
FDA Product Code
ODP FDA UDI
GMDN Term
Spinal fixation plate, non-bioabsorbable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3080 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

Yes

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
Sterilization Method
Radiation Sterilization FDA UDI

Category: Spinal fixation plate, non-bioabsorbable

Cervical Interbody 13mm x 12mm x 5mm Packaging by Xenco Medical Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Spinal fixation plate, non-bioabsorbable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Xenco Medical Llc

Sources (1)

  • FDA UDI 1e015ead-2ea7-4257-9ae3-fc35a8811139 33 fields · synced Jun 1, 2026