FDA UDI In Commercial Distribution 🇺🇸 United States

Curaplex

DI: 00817617020389 · Model: 680154-KIT · BOUND TREE MEDICAL, LLC
Product Codes
1
GMDN Terms
2
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Curaplex
Primary DI
00817617020389
Version / Model
680154-KIT
Catalog Number
680154-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
2023-10-18
Public Version Status
Update
Public Device Record Key
45b6215f-8685-4658-852a-f5326185a3de

Device Description

Curaplex Epi Kit incl 1 cc Syringe w/25 ga x 1 in Needle

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
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
FMF Syringe, piston

GMDN Terms

Code Name
34864 Adhesive bandage
17988 Antiseptic skin towelette

Identifiers

Type ID
Primary 00817617020389
Package 00810094571894