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4.0 X 125mm Tap

FDA UDI

Class I (US FDA UDI)

by OsteoCentric Technologies, Inc

Identity

Trade Name
4.0 X 125MM TAP FDA UDI
Generic Name
Bone tap, reusable FDA UDI
Device Name
4.0 X 125MM TAP FDA UDI
Model / Reference
303-4012 FDA UDI
Description
4.0 X 125MM TAP FDA UDI

Identifiers

Catalog Number
303-4012 FDA UDI
Primary DI / UDI-DI
00816950029899 FDA UDI
510(k) Number
K160603 FDA UDI
FDA Product Code
HWX FDA UDI
GMDN Term
Bone tap, reusable 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

No

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI
MRI Safety
MR Conditional FDA UDI

Dimensions & Sizes

Size
Outer Diameter — 4.0 Millimeter FDA UDI
Length — 125 Millimeter FDA UDI

Category: Bone tap, reusable

4.0 X 125mm Tap by OsteoCentric Technologies, Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bone tap, reusable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 0b4bd21b-e91b-4252-a2e5-81a3437ce1e9 37 fields · synced May 30, 2026