FDA UDI In Commercial Distribution 🇺🇸 United States

zRIP DuraBelt

DI: 00606959010482 · Model: ZRIP DURABELT · Respironics, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
zRIP DuraBelt
Primary DI
00606959010482
Version / Model
ZRIP DURABELT
Catalog Number
1075968
Company Name
Respironics, Inc.
Labeler DUNS
080728314
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-18
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
3029ecc5-7291-4762-b63a-30465398ad3b
Distribution End Date
9999-12-31

Device Description

zRIP Durabelt Kit, Adult, QDC

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
MNR VENTILATORY EFFORT RECORDER

GMDN Terms

Code Name
33843 Polysomnograph

Identifiers

Type ID
Primary 00606959010482

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K013905 000

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
-20 – 60 Degrees Celsius
Type
Storage Environment Humidity
Temperature Range
15 – 95 Percent (%) Relative Humidity
Type
Storage Environment Temperature
Temperature Range
-4 – 140 Degrees Fahrenheit