FDA UDI Not in Commercial Distribution 🇺🇸 United States

BodyMed

DI: 00815991025068 · Model: BDMRNK · BOXOUT, LLC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
BodyMed
Primary DI
00815991025068
Version / Model
BDMRNK
Company Name
BOXOUT, LLC
Labeler DUNS
066689993
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-08-14
Public Version
3
Public Version Date
2023-09-28
Public Version Status
Update
Public Device Record Key
b5926111-a17c-4e34-9558-a2ff21fb9802
Distribution End Date
2023-09-28

Device Description

BodyMed Reusable Nebulizer Kit including reusable nebulizer bottle,T connector, mouth piece, 2M oxygen tube, corrugated tube

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
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
Yes
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
CAF Nebulizer (Direct Patient Interface)

GMDN Terms

Code Name
62042 Nebulizing system delivery set, reusable

Identifiers

Type ID
Package 20815991025062
Primary 00815991025068