FDA UDI In Commercial Distribution 🇺🇸 United States

Curaplex

DI: 00815277021579 · Model: 670063-KIT · BOUND TREE MEDICAL, LLC
Product Codes
3
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Curaplex
Primary DI
00815277021579
Version / Model
670063-KIT
Catalog Number
670063-KIT
Company Name
BOUND TREE MEDICAL, LLC
Labeler DUNS
070556204
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-12-14
Public Version
4
Public Version Date
2022-08-16
Public Version Status
Update
Public Device Record Key
dc6727d4-b310-417d-861f-98bed49fd879

Device Description

Curaplex IV Start Kit w/ Tegaderm, Skin Prep, Ext Set, Flush

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
Combination Product
No
HCT/P
No
Contains NRL
Yes
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
FOZ Catheter,intravascular,therapeutic,short-term less than 30 days
POQ Blood transfusion kit
LRS I.V. start kit

GMDN Terms

Code Name
33963 Peripheral intravenous catheterization support kit

Identifiers

Type ID
Primary 00815277021579
Package 00810094570729