FDA UDI In Commercial Distribution 🇺🇸 United States

Kobold® Vaginal Cylinder Applicator Set (E)

DI: 00815568020076 · Model: 715-000 · KOBOLD, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Kobold® Vaginal Cylinder Applicator Set (E)
Primary DI
00815568020076
Version / Model
715-000
Company Name
KOBOLD, LLC
Labeler DUNS
014292258
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-23
Public Version
4
Public Version Date
2019-12-16
Public Version Status
Update
Public Device Record Key
8a4cbb3c-a7ab-40dd-9ebc-3077d687e74a

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
MR Unsafe
Direct Marking Exempt
No
PM Exempt
No
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
JAQ System, Applicator, Radionuclide, Remote-Controlled

GMDN Terms

Code Name
38407 Vaginal brachytherapy system applicator, remote-afterloading

Identifiers

Type ID
Primary 00815568020076