FDA UDI In Commercial Distribution 🇺🇸 United States

Curaplex

DI: 00812277032055 · Model: 301-44F10-120 · BOUND TREE MEDICAL, LLC
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
Curaplex
Primary DI
00812277032055
Version / Model
301-44F10-120
Catalog Number
301-44F10-120
Company Name
BOUND TREE MEDICAL, LLC
Labeler DUNS
070556204
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-12-15
Public Version
3
Public Version Date
2023-09-11
Public Version Status
Update
Public Device Record Key
56ad3fa5-f232-4834-9b2c-ecf48537a5cb

Device Description

VibraPEP without T-piece Adapter

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
Labeling does not contain MRI Safety Information
Direct Marking Exempt
Yes
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
BWF SPIROMETER, THERAPEUTIC (INCENTIVE)

GMDN Terms

Code Name
43947 Positive pressure airway secretion-clearing device

Identifiers

Type ID
Package 00812277032079
Package 00812277032062
Primary 00812277032055