FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 10886982077448 · Model: 03.231.016 · Synthes GmbH
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
10886982077448
Version / Model
03.231.016
Catalog Number
03231016
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
2022-04-28
Public Version Status
Update
Public Device Record Key
e03352a1-d3ce-42cf-a98b-6f25d06615be

Device Description

CANNULATED 4.0MM HEX SCRWDRVR SHAFT/6MM HEX COUPLING/180MM

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
HXX SCREWDRIVER

GMDN Terms

Code Name
33968 Surgical screwdriver, reusable

Identifiers

Type ID
Direct Marking 07611819457744
Secondary H679032310160
Primary 10886982077448

Customer Contacts