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Decima Spine Instrument Kit

FDA UDI

Class I (US FDA UDI)

by Decima Spine, Inc.

Identity

Trade Name
Decima Spine Instrument Kit FDA UDI
Generic Name
Orthopaedic bone screw starter/notcher FDA UDI
Device Name
Tap FDA UDI
Model / Reference
6119 FDA UDI
Description
Tap FDA UDI

Identifiers

Catalog Number
6119 FDA UDI
Primary DI / UDI-DI
00857360007091 FDA UDI
FDA Product Code
HWX FDA UDI
GMDN Term
Orthopaedic bone screw starter/notcher 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

No

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

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Orthopaedic bone screw starter/notcher

Decima Spine Instrument Kit by Decima Spine, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic bone screw starter/notcher.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Decima Spine, Inc.

Sources (1)

  • FDA UDI 51f7d7d0-d931-41c1-94e4-283eeaba6a3f 35 fields · synced May 30, 2026