FDA UDI In Commercial Distribution 🇺🇸 United States

EOlife

DI: 13770016085066 · Model: AUS00055 · ARCHEON
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
EOlife
Primary DI
13770016085066
Version / Model
AUS00055
Company Name
ARCHEON
Labeler DUNS
270625868
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-07-27
Public Version
1
Public Version Date
2023-08-04
Public Version Status
New
Public Device Record Key
ff528266-142e-4568-a3d1-289f686fc18c

Device Description

EOlife device (ref: AUS00055) is the sale reference of final medical device including : - EOlife ECU (ref: AUS00004) - EOlife BP (ref: A0000023) - EOlife Charger (ref: A0000063) - EOlife IFU (ref: AUS00057)

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
MR Unsafe
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
Yes
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
BTM Ventilator, Emergency, Manual (Resuscitator)

GMDN Terms

Code Name
17591 Pulmonary resuscitator, manual, reusable

Identifiers

Type ID
Primary 13770016085066

Premarket Submissions

Submission Number Supplement Number
K221841 000