FDA UDI In Commercial Distribution 🇺🇸 United States

Curaplex

DI: 00812277037562 · Model: 3246-95204 · BOUND TREE MEDICAL, LLC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Curaplex
Primary DI
00812277037562
Version / Model
3246-95204
Catalog Number
3246-95204
Company Name
BOUND TREE MEDICAL, LLC
Labeler DUNS
070556204
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-12-30
Public Version
1
Public Version Date
2023-01-09
Public Version Status
New
Public Device Record Key
162bef5b-d94f-46c0-b4d1-358f2e8a3778

Device Description

Curaplex Patient Mover Plus 1/EA 10EA/CS

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
Yes
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
FMR DEVICE, TRANSFER, PATIENT, MANUAL

GMDN Terms

Code Name
46148 Patient transfer system, manual

Identifiers

Type ID
Package 00812277038828
Primary 00812277037562