FDA UDI In Commercial Distribution 🇺🇸 United States

QUIKFLAP

DI: 07613154126682 · Model: 12-01500 · Stryker Leibinger GmbH & Co. KG
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
QUIKFLAP
Primary DI
07613154126682
Version / Model
12-01500
Catalog Number
12-01500
Company Name
Stryker Leibinger GmbH & Co. KG
Labeler DUNS
316153956
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-24
Public Version
5
Public Version Date
2023-09-18
Public Version Status
Update
Public Device Record Key
769e16a4-7271-40f6-8a9d-9a6b221858f6

Device Description

2 HOLE PLATES(3) SELF DRILLING SCREW(6)

Device Characteristics

Single Use
Yes
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
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
JEY PLATE, BONE

GMDN Terms

Code Name
46642 Craniofacial fixation plate, non-bioabsorbable, non-customized

Identifiers

Type ID
Primary 07613154126682

Premarket Submissions

Submission Number Supplement Number
K862482 000