FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 20887587017409 · Model: 04.501.114.05 · Synthes GmbH
Product Codes
2
GMDN Terms
1
Identifiers
3
Pkg Device Count
5

Basic Information

Brand Name
NA
Primary DI
20887587017409
Version / Model
04.501.114.05
Catalog Number
0450111405
Company Name
Synthes GmbH
Labeler DUNS
486711679
Distribution Status
In Commercial Distribution
Device Count in Pkg
5
Record Status
Published
Publish Date
2015-09-14
Public Version
4
Public Version Date
2022-04-25
Public Version Status
Update
Public Device Record Key
71d3f367-06a1-45c4-9078-f0949ec42daa

Device Description

3.0MM TI STERNAL LCKNG SCREW SELF-DRILLING/14MM

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
No
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
HWC Screw, fixation, bone

GMDN Terms

Code Name
34017 Sternal fixation device

Identifiers

Type ID
Secondary H98004501114050
Primary 20887587017409
Unit of Use 80887587017401

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K081700 000
K093772 000