FDA UDI In Commercial Distribution 🇺🇸 United States

Curaplex

DI: 00818834028622 · Model: 301-44F50-100 · TRI-ANIM HEALTH SERVICES, INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

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Basic Information

Brand Name
Curaplex
Primary DI
00818834028622
Version / Model
301-44F50-100
Catalog Number
301-44F50-100
Company Name
TRI-ANIM HEALTH SERVICES, INC.
Labeler DUNS
010712461
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-03-10
Public Version
1
Public Version Date
2024-03-18
Public Version Status
New
Public Device Record Key
c89330eb-005a-4ece-b6c4-589726b7a617

Device Description

VibraPEP Oscillatory PEP Therapy Device

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
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
No
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
BWF SPIROMETER, THERAPEUTIC (INCENTIVE)

GMDN Terms

Code Name
43947 Positive pressure airway secretion-clearing device

Identifiers

Type ID
Package 00818834028684
Package 00818834028653
Primary 00818834028622