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Neo Medical Cage kit

FDA UDI

Class II (US FDA UDI)

by Neo Medical Inc.

Identity

Trade Name
Neo Medical Cage kit FDA UDI
Generic Name
Internal spinal fixation procedure kit, single-use FDA UDI
Device Name
Cage Instrument Kit FDA UDI
Model / Reference
CI-00-00-00 FDA UDI
Description
Cage Instrument Kit FDA UDI

Identifiers

Primary DI / UDI-DI
07640177822000 FDA UDI
FDA Product Code
LHX FDA UDI
GMDN Term
Internal spinal fixation procedure kit, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.5800 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Internal spinal fixation procedure kit, single-use

Neo Medical Cage kit by Neo Medical Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Internal spinal fixation procedure kit, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Neo Medical Inc.

Sources (1)

  • FDA UDI ffa51a03-77ea-4c8b-b04d-c5ec06dde045 34 fields · synced May 31, 2026