FDA UDI In Commercial Distribution 🇺🇸 United States

Curaplex

DI: 00815277021128 · Model: 51089 · BOUND TREE MEDICAL, LLC
Product Codes
2
GMDN Terms
3
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Curaplex
Primary DI
00815277021128
Version / Model
51089
Catalog Number
51089
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
3
Public Version Date
2022-08-16
Public Version Status
Update
Public Device Record Key
13dc3535-80b8-4584-95a8-62e7bdf033aa

Device Description

Curaplex EMT Student Kit

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
CBP Valve, non-rebreathing
DXQ blood pressure cuff

GMDN Terms

Code Name
13755 Mechanical stethoscope
16156 Aneroid manual sphygmomanometer
61326 Cardiopulmonary resuscitation mask, single-use

Identifiers

Type ID
Primary 00815277021128
Package 00810071639074