FDA UDI In Commercial Distribution 🇺🇸 United States

Sleepiz One+

DI: 07649996477019 · Model: 1.0 · Sleepiz AG
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Sleepiz One+
Primary DI
07649996477019
Version / Model
1.0
Company Name
Sleepiz AG
Labeler DUNS
480221620
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-05-14
Public Version
1
Public Version Date
2024-05-22
Public Version Status
New
Public Device Record Key
032c4c44-ea92-40c3-af81-82a49aaf03b9

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
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
BZQ Monitor, Breathing Frequency
DRT Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)

GMDN Terms

Code Name
65669 Multiple vital physiological parameter monitoring system, home-use

Identifiers

Type ID
Primary 07649996477019

Premarket Submissions

Submission Number Supplement Number
K223163 000