FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 04546540500229 · Model: 0407281000 · STRYKER CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
04546540500229
Version / Model
0407281000
Catalog Number
0407281000
Company Name
STRYKER CORPORATION
Labeler DUNS
196548481
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-23
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
a002ca5e-3e07-4c46-855b-cc91016c523a

Device Description

Percutaneous Discectomy Probe

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
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
HRX ARTHROSCOPE

GMDN Terms

Code Name
36077 Diskectomy system, percutaneous, automatic

Identifiers

Type ID
Primary 04546540500229

Customer Contacts

Device Sizes

Type Value Unit Text
Length 3.0 Inch
Needle Gauge 19.0 Gauge

Storage Conditions

Type
Storage Environment Humidity
Temperature Range
10 – 75 Percent (%) Relative Humidity
Type
Storage Environment Atmospheric Pressure
Temperature Range
50 – 106 KiloPascal
Type
Storage Environment Temperature
Temperature Range
-20 – 40 Degrees Celsius