FDA UDI Not in Commercial Distribution 🇺🇸 United States

RF MultiGen

DI: 07613154578443 · Model: 0406900000 · STRYKER CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
RF MultiGen
Primary DI
07613154578443
Version / Model
0406900000
Catalog Number
0406-900-000
Company Name
STRYKER CORPORATION
Labeler DUNS
196548481
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-23
Public Version
10
Public Version Date
2022-06-10
Public Version Status
Update
Public Device Record Key
9f75d23a-39fe-4546-a318-68edcb4e6edc
Distribution End Date
2021-07-16

Device Description

Interventional Spine Generator

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

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
GEI ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES

GMDN Terms

Code Name
35156 Percutaneous radio-frequency ablation system generator

Identifiers

Type ID
Primary 07613154578443

Customer Contacts

Storage Conditions

Type
Storage Environment Humidity
Temperature Range
10 – 75 Percent (%) Relative Humidity
Type
Storage Environment Temperature
Temperature Range
-34 – 65 Degrees Celsius
Type
Storage Environment Atmospheric Pressure
Temperature Range
50 – 106 KiloPascal