FDA UDI In Commercial Distribution 🇺🇸 United States

PlusDrive

DI: 10887587042008 · Model: 400.038E · Synthes GmbH
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
PlusDrive
Primary DI
10887587042008
Version / Model
400.038E
Catalog Number
400038E
Company Name
Synthes GmbH
Labeler DUNS
486711679
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-14
Public Version
6
Public Version Date
2024-02-27
Public Version Status
Update
Public Device Record Key
d1899e0b-0952-4522-912c-1475ccc1a1f6

Device Description

1.5MM TI CORTEX SCR SLF-TPNG WITH PLUSDRIVE(TM) RECESS 8MM

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
DZL SCREW, FIXATION, INTRAOSSEOUS

GMDN Terms

Code Name
66947 Orthopaedic bone screw (non-sliding)

Identifiers

Type ID
Secondary H980400038E0
Primary 10887587042008

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K980199 000