FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 04046964327681 · Model: 610378 · B BRAUN INTERVENTIONAL SYSTEMS, INC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
5

Basic Information

Brand Name
NA
Primary DI
04046964327681
Version / Model
610378
Catalog Number
610378
Company Name
B BRAUN INTERVENTIONAL SYSTEMS, INC
Labeler DUNS
784259751
Distribution Status
In Commercial Distribution
Device Count in Pkg
5
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
73e6bbdd-436b-4466-b1d2-b2325b9641e0

Device Description

5F MPK 4CM NDL-018 NT GW SS 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 04046964327681
Unit of Use 04046964327667

Customer Contacts

Storage Conditions

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