FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 07613252213260 · Model: 5901-1200 · Stryker Trauma SA
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
07613252213260
Version / Model
5901-1200
Catalog Number
5901-1200
Company Name
Stryker Trauma SA
Labeler DUNS
481999654
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-04-07
Public Version
5
Public Version Date
2023-06-12
Public Version Status
Update
Public Device Record Key
7e4ff11a-bc9d-419f-b530-93096bf486c5

Device Description

Tray

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
LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

GMDN Terms

Code Name
47831 Orthopaedic implantation sleeve, reusable

Identifiers

Type ID
Primary 07613252213260