FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 04046964327025 · Model: 610361 · B BRAUN INTERVENTIONAL SYSTEMS, INC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
10

Basic Information

Brand Name
NA
Primary DI
04046964327025
Version / Model
610361
Catalog Number
610361
Company Name
B BRAUN INTERVENTIONAL SYSTEMS, INC
Labeler DUNS
784259751
Distribution Status
In Commercial Distribution
Device Count in Pkg
10
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
4876ebe8-7864-4666-9740-c701a7294338

Device Description

4F MPK 7 CM NDL-018 NT GW PT TIP-STD

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
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
DRE DILATOR, VESSEL, FOR PERCUTANEOUS CATHETERIZATION

GMDN Terms

Code Name
58865 Vascular catheter introduction set, nonimplantable

Identifiers

Type ID
Primary 04046964327025
Unit of Use 04046964327001

Customer Contacts

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Store at room temp
Type
Special Storage Condition, Specify