FDA UDI In Commercial Distribution 🇺🇸 United States

PlusDrive

DI: 10887587036748 · Model: 313.805 · Synthes GmbH
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
PlusDrive
Primary DI
10887587036748
Version / Model
313.805
Catalog Number
313805
Company Name
Synthes GmbH
Labeler DUNS
486711679
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-12-31
Public Version
5
Public Version Date
2022-04-25
Public Version Status
Update
Public Device Record Key
47aa1cec-88a7-44cf-bb91-578ca8c09b17

Device Description

1.3MM SCREWDRIVER BLADE HXC SLF-RETAIN PLUSDRIVE(TM) 52MM

Device Characteristics

Single Use
No
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
Yes
PM Exempt
Yes
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
HXX SCREWDRIVER

GMDN Terms

Code Name
33968 Surgical screwdriver, reusable

Identifiers

Type ID
Secondary H9803138050
Primary 10887587036748

Customer Contacts