FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 04546540195890 · Model: 1806-0080S · Stryker Trauma SA
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
04546540195890
Version / Model
1806-0080S
Catalog Number
1806-0080S
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
6
Public Version Date
2023-09-18
Public Version Status
Update
Public Device Record Key
a91912d8-ee76-43d7-bb8e-e267fc84d78b

Device Description

Guide Wire, Ball-Tipped, 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
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
MAY Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous cemented, osteophilic finish

GMDN Terms

Code Name
46165 Orthopaedic guidewire, reusable

Identifiers

Type ID
Primary 04546540195890

Device Sizes

Type Value Unit Text
Length 800.0 Millimeter
Device Size Text, specify Diameter: 3.0 Millimeter