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Black Diamond Pedicle Screw System

FDA UDI

Class II (US FDA UDI)

by Osseus Fusion Systems Llc

Identity

Trade Name
Black Diamond Pedicle Screw System FDA UDI
Generic Name
Surgical instrument handle, non-torque-limiting FDA UDI
Device Name
T-HANDLE QUICK CONNECT RATCHET HANDLE (OUT) FDA UDI
Model / Reference
1010-1013 FDA UDI
Description
T-HANDLE QUICK CONNECT RATCHET HANDLE (OUT) FDA UDI

Identifiers

Catalog Number
1010-1013 FDA UDI
Primary DI / UDI-DI
B06210101013 FDA UDI
FDA Product Code
MNH FDA UDI
MNI FDA UDI
GMDN Term
Surgical instrument handle, non-torque-limiting FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3070 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

Category: Surgical instrument handle, non-torque-limiting

Black Diamond Pedicle Screw System by Osseus Fusion Systems Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical instrument handle, non-torque-limiting.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI f7f8b45f-6c59-4706-a842-4b6f25692b39 35 fields · synced Jun 1, 2026