← Back to catalogue

Futura

FDA UDI

Class I (US FDA UDI)

by Tornier, Inc.

Identity

Trade Name
Futura FDA UDI
Generic Name
Surgical instrument handle, non-torque-limiting FDA UDI
Device Name
UNIVERSAL HANDLE FDA UDI
Model / Reference
MHT-LGTH FDA UDI
Description
UNIVERSAL HANDLE FDA UDI

Identifiers

Catalog Number
MHT-LGTH FDA UDI
Primary DI / UDI-DI
00846832018055 FDA UDI
FDA Product Code
LXH FDA UDI
GMDN Term
Surgical instrument handle, non-torque-limiting 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

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 instrument handle, non-torque-limiting

Futura by Tornier, Inc. — Class I — 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Tornier, Inc.

Sources (1)

  • FDA UDI 490179ca-7219-440e-a401-1013502546a6 35 fields · synced Jun 6, 2026