FDA UDI In Commercial Distribution 🇺🇸 United States

APEX

DI: 04713025000134 · Model: 9S-007200 · Wellell Inc.
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
APEX
Primary DI
04713025000134
Version / Model
9S-007200
Company Name
Wellell Inc.
Labeler DUNS
656413127
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-23
Public Version
4
Public Version Date
2024-06-28
Public Version Status
Update
Public Device Record Key
b8d9c4ac-d4ca-4dce-b916-e97d52850c0c

Device Description

iCH Auto

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
BZD Ventilator, Non-Continuous (Respirator)

GMDN Terms

Code Name
60711 Home CPAP unit

Identifiers

Type ID
Primary 04713025000134
Package 14713025000131

Premarket Submissions

Submission Number Supplement Number
K141522 000