FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 10886982079800 · Model: 03.401.070 · Synthes GmbH
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
10886982079800
Version / Model
03.401.070
Catalog Number
03401070
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
2023-01-20
Public Version Status
Update
Public Device Record Key
5e7fea09-8449-444a-b8e7-22464cbefbff

Device Description

GUIDE BAR FOR REMOVAL OF IMPLANTS

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
HWB EXTRACTOR

GMDN Terms

Code Name
32856 Orthopaedic implant impactor, reusable

Identifiers

Type ID
Direct Marking 07611819408654
Secondary H679034010700
Primary 10886982079800

Customer Contacts