FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 10886982199010 · Model: 393.103 · Synthes GmbH
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
10886982199010
Version / Model
393.103
Catalog Number
393103
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
4
Public Version Date
2022-05-02
Public Version Status
Update
Public Device Record Key
ec35e09e-7d6f-4d76-b5b9-27b57b3bee4b

Device Description

DRIVE ADAPTOR WITH QC FOR 5.0MM SCHANZ SCREWS

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
No
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
GFC DRIVER, SURGICAL, PIN

GMDN Terms

Code Name
36235 Manual surgical rotary handpiece, reusable

Identifiers

Type ID
Direct Marking 07611819775770
Secondary H6793931030
Primary 10886982199010

Customer Contacts