FDA UDI In Commercial Distribution 🇺🇸 United States

Hobbs Biliary Amsterdam Stent

DI: M84961120 · Model: 6112 · HOBBS MEDICAL, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Hobbs Biliary Amsterdam Stent
Primary DI
M84961120
Version / Model
6112
Catalog Number
6112
Company Name
HOBBS MEDICAL, INC.
Labeler DUNS
076769355
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-21
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
eba99842-1bbb-442a-be48-1388441ed3e4

Device Description

A sterile non-bioabsorbable tubular device intended to be implanted in an obstructed biliary duct (e.g., common bile duct) to maintain luminal patency. It is made entirely of a synthetic polymer designed as a continuous tube with retention flanges. Single use device.

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
Yes
MRI Safety
MR Safe
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
43764 Polymeric biliary stent, non-bioabsorbable

Identifiers

Type ID
Primary M84961120

Customer Contacts

Phone
8606845875

Premarket Submissions

Submission Number Supplement Number
K834351 000