FDA UDI In Commercial Distribution 🇺🇸 United States

NIGHTOWL

DI: 09353645351022 · Model: 35102 · RESMED ASIA PTE. LTD.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NIGHTOWL
Primary DI
09353645351022
Version / Model
35102
Company Name
RESMED ASIA PTE. LTD.
Labeler DUNS
659298251
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-08-04
Public Version
1
Public Version Date
2025-08-12
Public Version Status
New
Public Device Record Key
eaa1684b-44e8-4bb2-9f4e-737b7b5cb162

Device Description

NIGHTOWL USA

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
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
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
MNR Ventilatory Effort Recorder

GMDN Terms

Code Name
12391 Wearable multiple physiological parameter recorder, reusable

Identifiers

Type ID
Primary 09353645351022

Storage Conditions

Type
Handling Environment Humidity
Temperature Range
20 – 95 Percent (%) Relative Humidity
Type
Handling Environment Temperature
Temperature Range
-4 – 140 Degrees Fahrenheit