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Neo Medical Cage kit

FDA UDI

Class I (US FDA UDI)

by Neo Medical Inc.

Identity

Trade Name
Neo Medical Cage kit FDA UDI
Generic Name
Bone file/rasp, manual, single-use FDA UDI
Device Name
Scraper/distractor 9 mm XL FDA UDI
Model / Reference
CI-SD-09-XL FDA UDI
Description
Scraper/distractor 9 mm XL FDA UDI

Identifiers

Primary DI / UDI-DI
07640177822284 FDA UDI
FDA Product Code
LXH FDA UDI
GMDN Term
Bone file/rasp, manual, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 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

No

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

Dimensions & Sizes

Size
Length — 9 Millimeter FDA UDI

Category: Bone file/rasp, manual, single-use

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

Similar devices

Also classified as Bone file/rasp, manual, 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 48f58d75-8337-4063-a686-52fdc6c24e1b 35 fields · synced Jun 8, 2026