FDA UDI In Commercial Distribution 🇺🇸 United States

Curaplex

DI: 00810094573850 · Model: 670248-KIT · BOUND TREE MEDICAL, LLC
Product Codes
1
GMDN Terms
2
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Curaplex
Primary DI
00810094573850
Version / Model
670248-KIT
Catalog Number
670248-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
2022-07-30
Public Version
1
Public Version Date
2022-08-08
Public Version Status
New
Public Device Record Key
18c7b159-7be5-48e9-9b8e-603b274427df

Device Description

Curaplex CPR AED Responder Kit, Heartsmart

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
CBP Valve, non-rebreathing

GMDN Terms

Code Name
36066 Cardiopulmonary resuscitation mask, reusable
43000 First aid kit, non-medicated, reusable

Identifiers

Type ID
Primary 00810094573850