← Back to catalogue

Loqteq®

FDA UDI

Class I (US FDA UDI)

by aap Implantate AG

Identity

Trade Name
LOQTEQ® FDA UDI
Generic Name
Orthopaedic implant aiming/guiding block attachment tool FDA UDI
Device Name
Aiming device LOQTEQ Distal Femur Plate, L FDA UDI
Model / Reference
IU 8189-02 FDA UDI
Description
Aiming device LOQTEQ Distal Femur Plate, L FDA UDI

Identifiers

Primary DI / UDI-DI
04042409346064 FDA UDI
FDA Product Code
LXH FDA UDI
GMDN Term
Orthopaedic implant aiming/guiding block attachment tool 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

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Orthopaedic implant aiming/guiding block attachment tool

Loqteq® by aap Implantate AG — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic implant aiming/guiding block attachment tool.

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
aap Implantate AG

Sources (1)

  • FDA UDI 61ec6006-5981-4b81-8110-b8fcd055d614 33 fields · synced May 31, 2026