FDA UDI In Commercial Distribution 🇺🇸 United States

Z-MED™

DI: 04046964338489 · Model: 611812 · B BRAUN INTERVENTIONAL SYSTEMS, INC
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Z-MED™
Primary DI
04046964338489
Version / Model
611812
Catalog Number
611812
Company Name
B BRAUN INTERVENTIONAL SYSTEMS, INC
Labeler DUNS
784259751
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-08-09
Public Version
5
Public Version Date
2023-09-07
Public Version Status
Update
Public Device Record Key
72860d42-ce21-4b70-be4e-44583fc7159b

Device Description

SO052 Z-MED 23X2X120

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
LIT Catheter, angioplasty, peripheral, transluminal
OZT Balloon aortic valvuloplasty

GMDN Terms

Code Name
17453 Cardiac valvuloplasty catheter

Identifiers

Type ID
Primary 04046964338489

Customer Contacts

Storage Conditions

Type
Special Storage Condition, Specify
Type
Special Storage Condition, Specify
Special Conditions
Keep away from sunlight
Type
Special Storage Condition, Specify
Special Conditions
Store at room temp