FDA UDI In Commercial Distribution 🇺🇸 United States

Aerobika,OPEP

DI: 00604351505124 · Model: Aerobika, OPEP Device, Retail · Monaghan Medical Corporation
Product Codes
1
GMDN Terms
1
Identifiers
4
Pkg Device Count
1

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Basic Information

Brand Name
Aerobika,OPEP
Primary DI
00604351505124
Version / Model
Aerobika, OPEP Device, Retail
Company Name
Monaghan Medical Corporation
Labeler DUNS
056332380
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-05-16
Public Version
2
Public Version Date
2025-03-25
Public Version Status
Update
Public Device Record Key
ad30c5a3-4198-4620-915a-9ea672d5f1a4

Device Description

AEROBIKA, OPEP DEVICE, RETAIL- 50512

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
Yes
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
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
BWF Spirometer, Therapeutic (Incentive)

GMDN Terms

Code Name
43947 Positive pressure airway secretion-clearing device

Identifiers

Type ID
Package 50604351505129
Primary 00604351505124
Package 60604351505126
Package 70604351505123

Customer Contacts

Phone
518-561-7330

Premarket Submissions

Submission Number Supplement Number
K123400 000