FDA UDI In Commercial Distribution 🇺🇸 United States

HOFFMANN

DI: 07613252610762 · Model: 4933-4-155 · Stryker Trauma SA
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
HOFFMANN
Primary DI
07613252610762
Version / Model
4933-4-155
Catalog Number
4933-4-155
Company Name
Stryker Trauma SA
Labeler DUNS
481999654
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-22
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
0d2e1db7-f736-47c5-9039-8276f825aa01

Device Description

Segment Ring LRF

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
No
PM Exempt
No
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
KTT APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT

GMDN Terms

Code Name
35647 External orthopaedic fixation system, reusable

Identifiers

Type ID
Primary 07613252610762

Device Sizes

Type Value Unit Text
Device Size Text, specify Diameter: 155.0 Millimeter