FDA UDI In Commercial Distribution 🇺🇸 United States

LOQTEQ®

DI: 04042409388682 · Model: PH 3534-02-2 · aap Implantate AG
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
LOQTEQ®
Primary DI
04042409388682
Version / Model
PH 3534-02-2
Company Name
aap Implantate AG
Labeler DUNS
328420633
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-06-21
Public Version
2
Public Version Date
2024-02-19
Public Version Status
Update
Public Device Record Key
1aacfe2e-7533-45c7-8ea2-46dcde92d600

Device Description

LOQTEQ® VA Distal Dorsolateral Humerus Plate, 2 holes, L 89, L, Titanium

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
Yes
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
HRS Plate, Fixation, Bone

GMDN Terms

Code Name
61689 Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile

Identifiers

Type ID
Primary 04042409388682

Premarket Submissions

Submission Number Supplement Number
K230141 000