FDA UDI In Commercial Distribution 🇺🇸 United States

CELSITE

DI: 04046963594954 · Model: 5433750 · B BRAUN INTERVENTIONAL SYSTEMS, INC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
CELSITE
Primary DI
04046963594954
Version / Model
5433750
Catalog Number
5433750
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
2015-07-29
Public Version
6
Public Version Date
2023-09-07
Public Version Status
Update
Public Device Record Key
bd8d23a1-9979-4a19-9e33-83838da87f6a

Device Description

CELSITE ST305 SM SET SIL 6,5F IV USA

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
LJT PORT & CATHETER, IMPLANTED, SUBCUTANEOUS, INTRAVASCULAR

GMDN Terms

Code Name
61494 Vascular port/catheter

Identifiers

Type ID
Primary 04046963594954

Customer Contacts

Device Sizes

Type Value Unit Text
Catheter Gauge 6.50 French
Device Size Text, specify Septum Diameter : 9.500 MM

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
KEEP DRY
Type
Special Storage Condition, Specify
Special Conditions
Store at room temp
Type
Special Storage Condition, Specify
Special Conditions
Avoid extreme temperature
Type
Special Storage Condition, Specify
Special Conditions
Keep away from sunlight
Type
Special Storage Condition, Specify