FDA UDI In Commercial Distribution 🇺🇸 United States

Silicone Biliary Stent

DI: 00684995500174 · Model: GR83064-13SP · BENTEC MEDICAL OPCO, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Silicone Biliary Stent
Primary DI
00684995500174
Version / Model
GR83064-13SP
Company Name
BENTEC MEDICAL OPCO, LLC
Labeler DUNS
080524654
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-01-03
Public Version
5
Public Version Date
2020-11-19
Public Version Status
Update
Public Device Record Key
62ac4056-043e-4d48-bb39-e08686b7d04a

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
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
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
FGE Catheter, Biliary, Diagnostic

GMDN Terms

Code Name
10696 Biliary drain

Identifiers

Type ID
Primary 00684995500174

Premarket Submissions

Submission Number Supplement Number
K844384 000