FDA UDI In Commercial Distribution 🇺🇸 United States

DRIVEMEDICAL

DI: 00822383286563 · Model: 18031 · Drive Devilbiss Healthcare
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
DRIVEMEDICAL
Primary DI
00822383286563
Version / Model
18031
Company Name
Drive Devilbiss Healthcare
Labeler DUNS
867673159
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-06-21
Public Version
3
Public Version Date
2025-09-24
Public Version Status
Update
Public Device Record Key
db143ebe-e8d5-4daa-bcd1-4b2e2096ca24

Device Description

RespiratoryCarts/racks/cases/stands Product Description: Nebulizer Carry Bag, 1/ea

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
No
PM Exempt
No
Has Serial Number
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
JCX APPARATUS, SUCTION, WARD USE, PORTABLE, AC-POWERED

GMDN Terms

Code Name
35457 Therapeutic agent nebulizer, benchtop

Identifiers

Type ID
Package 50822383286568
Primary 00822383286563

Premarket Submissions

Submission Number Supplement Number
K042349 000