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Loqteq®

FDA UDIEUDAMED

Class II (US FDA UDI)

Ref PU 3534-04-2Model Bone plates (non-sterile)

by aap Implantate AG

Identity

Trade Name
LOQTEQ® EUDAMEDFDA UDI
Generic Name
Orthopaedic fixation plate, non-bioabsorbable FDA UDI
Device Name
LOQTEQ® VA Olecranon Plate, 4 holes, L 112, L, Titanium FDA UDI
Model / Reference
PU 3534-04-2 EUDAMEDFDA UDI
Bone plates (non-sterile) EUDAMED
Description
LOQTEQ® VA Olecranon Plate, 4 holes, L 112, L, Titanium FDA UDI

Identifiers

Primary DI / UDI-DI
04042409389108 EUDAMEDFDA UDI
Basic UDI-DI
40424090161H6 EUDAMED
510(k) Number
K230141 FDA UDI
FDA Product Code
HRS FDA UDI
EMDN Code
P09120503 OSTEOSYNTHESIS SCREW-PLATE SYSTEMS EUDAMED
GMDN Term
Orthopaedic fixation plate, non-bioabsorbable FDA UDI

Classification

Device Class
Class IIb EUDAMED
Class II FDA UDI
Regulation Number
888.3030 FDA UDI
Market of Registration
Germany EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

Yes

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

Sutures

Yes

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

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

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Orthopaedic fixation plate, non-bioabsorbable

Loqteq® by aap Implantate AG — Class II — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic fixation plate, non-bioabsorbable.

Cleared under the same submission

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
aap Implantate AG

Sources (2)

  • FDA UDI a8b3276f-4780-4337-8014-c4b70c5a6e2b 34 fields · synced Oct 6, 2026
  • EUDAMED 01ffd944-9d3d-4374-a764-430147d8a40b 61 fields · synced Oct 6, 2026