FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 04546540039644 · Model: 0206711000 · STRYKER CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
04546540039644
Version / Model
0206711000
Catalog Number
0206711000
Company Name
STRYKER CORPORATION
Labeler DUNS
196548481
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-09-24
Public Version
1
Public Version Date
2018-10-25
Public Version Status
New
Public Device Record Key
e1b85a59-3fee-4605-860d-c0d973c1e479

Device Description

Femoral Canal Brush

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
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
GDY GAUZE/SPONGE, INTERNAL, X-RAY DETECTABLE

GMDN Terms

Code Name
45253 Orthopaedic cement preparation/delivery kit

Identifiers

Type ID
Package 34546540039645
Primary 04546540039644

Customer Contacts