FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 20705034711345 · Model: 02.600.022.10S · Synthes GmbH
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
10

Basic Information

Brand Name
NA
Primary DI
20705034711345
Version / Model
02.600.022.10S
Catalog Number
0260002210S
Company Name
Synthes GmbH
Labeler DUNS
486711679
Distribution Status
In Commercial Distribution
Device Count in Pkg
10
Record Status
Published
Publish Date
2018-10-31
Public Version
4
Public Version Date
2022-07-14
Public Version Status
Update
Public Device Record Key
bd28d145-0409-4049-a033-9efc92b127d2

Device Description

DISTRACTOR PINS 12MM-STERILE

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
Yes
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
HXW BENDER

GMDN Terms

Code Name
44759 General internal orthopaedic fixation system implantation kit

Identifiers

Type ID
Secondary H9810260002210S0
Primary 20705034711345
Unit of Use 80705034711347

Customer Contacts