FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 07613327122954 · Model: 56-90312 · Stryker Leibinger GmbH & Co. KG
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
07613327122954
Version / Model
56-90312
Catalog Number
56-90312
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
2017-03-31
Public Version
6
Public Version Date
2023-09-18
Public Version Status
Update
Public Device Record Key
bc6f323a-2d44-488a-b1c4-0aa20c39fbc3

Device Description

1,5/1,7MM DYNAMIC MESH-MALL-SMALL

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
MR Conditional
Direct Marking Exempt
No
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
GWO Plate, cranioplasty, preformed, alterable

GMDN Terms

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

Identifiers

Type ID
Primary 07613327122954

Premarket Submissions

Submission Number Supplement Number
K161821 000

Device Sizes

Type Value Unit Text
Device Size Text, specify Thickness: 0.3 Millimeter
Length 40.0 Millimeter
Width 40.0 Millimeter