FDA UDI In Commercial Distribution 🇺🇸 United States

Curaplex

DI: 00817617029122 · Model: 8600-01282 · BOUND TREE MEDICAL, LLC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Curaplex
Primary DI
00817617029122
Version / Model
8600-01282
Catalog Number
8600-01282
Company Name
BOUND TREE MEDICAL, LLC
Labeler DUNS
070556204
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-12-18
Public Version
4
Public Version Date
2022-08-16
Public Version Status
Update
Public Device Record Key
b4b90e38-aa3f-4320-81f5-5e73cf52d4d0

Device Description

IV Start Kit with Site-loc, Skin Prep, Gauze, TQ, Tape, 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
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
Yes
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
LRS I.V. start kit

GMDN Terms

Code Name
33963 Peripheral intravenous catheterization support kit

Identifiers

Type ID
Primary 00817617029122
Package 00810094572518