FDA UDI In Commercial Distribution 🇺🇸 United States

Curaplex

DI: 00817617025193 · Model: 1431-16012 · BOUND TREE MEDICAL, LLC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Curaplex
Primary DI
00817617025193
Version / Model
1431-16012
Catalog Number
1431-16012
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
8edec9ca-55e3-4dda-beb2-5c7a2be16b51

Device Description

Curaplex Hot Pack, Large

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
Kit
No
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
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
IDM MICROTOME, ULTRA

GMDN Terms

Code Name
37240 Hot/cold therapy pack, reusable

Identifiers

Type ID
Package 00817617025247
Primary 00817617025193