FDA UDI In Commercial Distribution 🇺🇸 United States

Curaplex

DI: 00817617026640 · Model: 2751-50487 · BOUND TREE MEDICAL, LLC
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
Curaplex
Primary DI
00817617026640
Version / Model
2751-50487
Catalog Number
2751-50487
Company Name
BOUND TREE MEDICAL, LLC
Labeler DUNS
070556204
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-09-04
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
2f75dbd1-f723-416c-962c-4222322f2845

Device Description

Curaplex 50mm X 48mm foam electrode, wet gel, 60 ea/pouch

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
Yes
MRI Safety
MR Unsafe
Direct Marking Exempt
No
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
DRX Electrode, electrocardiograph

GMDN Terms

Code Name
35035 Electrocardiographic electrode, single-use

Identifiers

Type ID
Package 00817617026602
Primary 00817617026640
Package 00817617026565