FDA UDI In Commercial Distribution 🇺🇸 United States

I-125 Seed

DI: 00815165020196 · Model: I-125 Seed · Eckert & Ziegler Bebig, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
I-125 Seed
Primary DI
00815165020196
Version / Model
I-125 Seed
Catalog Number
I125SEED
Company Name
Eckert & Ziegler Bebig, Inc.
Labeler DUNS
021125001
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-10-27
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
d2494c80-5e7e-4a37-b592-28eeee1a6e33

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
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
Yes
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
KXK Source, Brachytherapy, Radionuclide

GMDN Terms

Code Name
38299 Manual brachytherapy system

Identifiers

Type ID
Primary 00815165020196

Customer Contacts

Phone
203-262-0571