FDA UDI Not in Commercial Distribution 🇺🇸 United States

Cross-Screw

DI: 04546540756800 · Model: 234-500-201 · STRYKER CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Cross-Screw
Primary DI
04546540756800
Version / Model
234-500-201
Catalog Number
234-500-201
Company Name
STRYKER CORPORATION
Labeler DUNS
187502109
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-04
Public Version
8
Public Version Date
2023-04-04
Public Version Status
Update
Public Device Record Key
9abcbf9c-77c5-450e-b96a-c66faf6cef10
Distribution End Date
2018-12-07

Device Description

TRAY BASE FOR CROSS-SCREW INSTRUMENTATION SET

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
Ethylene Oxide

Product Codes

Code Name
FSM TRAY, SURGICAL, INSTRUMENT

GMDN Terms

Code Name
13730 Device sterilization/disinfection container, reusable

Identifiers

Type ID
Primary 04546540756800

Customer Contacts