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Made-To-Order

FDA UDI

Class I (US FDA UDI)

by Tornier, Inc.

Identity

Trade Name
Made-To-Order FDA UDI
Generic Name
Surgical screwdriver, reusable FDA UDI
Device Name
Perform Shoulder Depth Stop FDA UDI
Model / Reference
9027448 FDA UDI
Description
Perform Shoulder Depth Stop FDA UDI

Identifiers

Catalog Number
9027448 FDA UDI
Primary DI / UDI-DI
00846832097371 FDA UDI
FDA Product Code
GFG FDA UDI
GMDN Term
Surgical screwdriver, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4820 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: Surgical screwdriver, reusable

Made-To-Order by Tornier, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical screwdriver, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Tornier, Inc.

Sources (1)

  • FDA UDI e323aad5-fa0c-40cb-8302-6c7e211b7249 36 fields · synced May 30, 2026