FDA UDI In Commercial Distribution 🇺🇸 United States

PlusDrive

DI: 20887587042272 · Model: 400.058 · Synthes GmbH
Product Codes
4
GMDN Terms
1
Identifiers
3
Pkg Device Count
5

Basic Information

Brand Name
PlusDrive
Primary DI
20887587042272
Version / Model
400.058
Catalog Number
400058
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
5
Public Version Date
2023-02-03
Public Version Status
Update
Public Device Record Key
1c8c041f-ceb4-4c0a-b7ef-dfd6a94c253d

Device Description

1.5MM TI CORTEX SCR SLF-DRLG 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
JEY PLATE, BONE
DZL SCREW, FIXATION, INTRAOSSEOUS
MQN EXTERNAL MANDIBULAR FIXATOR AND/OR DISTRACTOR
PBJ Cranial Distraction System

GMDN Terms

Code Name
47635 Implantable craniofacial bone distractor

Identifiers

Type ID
Primary 20887587042272
Unit of Use 80887587042274
Secondary H9804000580

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K102656 000
K162594 000
K170818 000
K963546 000