FDA UDI In Commercial Distribution 🇺🇸 United States

HOFFMANN

DI: 04546540495129 · Model: 4941-2-120 · Stryker Trauma SA
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
HOFFMANN
Primary DI
04546540495129
Version / Model
4941-2-120
Catalog Number
4941-2-120
Company Name
Stryker Trauma SA
Labeler DUNS
481999654
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-24
Public Version
5
Public Version Date
2022-07-11
Public Version Status
Update
Public Device Record Key
008e2b3a-4ed9-40f6-b54e-9c1634fbcbc7

Device Description

Straight Post Compact 5mm

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
Yes
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
LXT APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT, METAL COMPOSITE
JEC COMPONENT, TRACTION, INVASIVE

GMDN Terms

Code Name
35647 External orthopaedic fixation system, reusable

Identifiers

Type ID
Primary 04546540495129