FDA UDI In Commercial Distribution 🇺🇸 United States

SleepmateRIPmate Kit - Integrated RIP Keyhole

DI: 05707480134021 · Model: 819100-108 · Ambu A/S
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
SleepmateRIPmate Kit - Integrated RIP Keyhole
Primary DI
05707480134021
Version / Model
819100-108
Catalog Number
819100-108
Company Name
Ambu A/S
Labeler DUNS
305682023
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-22
Public Version
4
Public Version Date
2018-10-29
Public Version Status
Update
Public Device Record Key
c87ff7d5-9d97-4a5b-ac64-bb9ef36f0a79

Device Description

RIPmate Kit - Integrated RIP Keyhole

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
Yes
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
BZQ Monitor, breathing frequency

GMDN Terms

Code Name
33843 Polysomnograph

Identifiers

Type ID
Primary 05707480134021
Direct Marking 05707480096831

Customer Contacts

Phone
+14107686464

Premarket Submissions

Submission Number Supplement Number
K903300 000