FDA UDI Not in Commercial Distribution 🇺🇸 United States

Carry Case Activox

DI: 09353645000081 · Model: 123-102 · RESMED ASIA PTE. LTD.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Carry Case Activox
Primary DI
09353645000081
Version / Model
123-102
Company Name
RESMED ASIA PTE. LTD.
Labeler DUNS
659276906
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-07-27
Public Version
6
Public Version Date
2023-07-31
Public Version Status
Update
Public Device Record Key
c922dc0c-5d6e-4134-9ba3-0423c5140ec0
Distribution End Date
2023-07-30

Device Description

Carry Case, Universal, Activox

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
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
CAW Generator, Oxygen, Portable

GMDN Terms

Code Name
37685 Personal device holder, reusable

Identifiers

Type ID
Primary 09353645000081

Customer Contacts

Phone
800-427-0737