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Neo Medical Pedicle Screw System

FDA UDI

Class I (US FDA UDI)

by Neo Medical Inc.

Identity

Trade Name
Neo Medical Pedicle Screw System FDA UDI
Generic Name
Bone tap, single-use FDA UDI
Device Name
Tap kit diameter 7.0 FDA UDI
Model / Reference
TP-70-00-00 FDA UDI
Description
Tap kit diameter 7.0 FDA UDI

Identifiers

Primary DI / UDI-DI
07640177820488 FDA UDI
FDA Product Code
HWX FDA UDI
GMDN Term
Bone tap, 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
Outer Diameter — 7.0 Millimeter FDA UDI

Category: Bone tap, single-use

Neo Medical Pedicle Screw System by Neo Medical Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bone tap, 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 b206503d-2db4-4c48-9d0e-5c8f73a9795a 35 fields · synced May 30, 2026