FDA UDI Not in Commercial Distribution 🇺🇸 United States

Mini Ghost™

DI: 04046964345159 · Model: 612687 · B BRAUN INTERVENTIONAL SYSTEMS, INC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Mini Ghost™
Primary DI
04046964345159
Version / Model
612687
Catalog Number
612687
Company Name
B BRAUN INTERVENTIONAL SYSTEMS, INC
Labeler DUNS
784259751
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-08-09
Public Version
8
Public Version Date
2022-11-02
Public Version Status
Update
Public Device Record Key
ef494c69-17f9-4f88-a54f-1065d1f93735
Distribution End Date
2021-08-04

Device Description

MG224 MINI GHOST 4MM X 10CM X 40CM

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
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
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
DQY CATHETER, PERCUTANEOUS

GMDN Terms

Code Name
17184 Peripheral angioplasty balloon catheter, basic

Identifiers

Type ID
Primary 04046964345159

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K051343 000

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
ROOM TEMP AWAY FROM SUNLIGHT
Type
Special Storage Condition, Specify