FDA UDI In Commercial Distribution 🇺🇸 United States

Oxus Refurbished Sieve Bed

DI: 00867460000120 · Model: RS-07001/RS-07002 · OXUS AMERICA, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Oxus Refurbished Sieve Bed
Primary DI
00867460000120
Version / Model
RS-07001/RS-07002
Company Name
OXUS AMERICA, INC.
Labeler DUNS
962894098
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-06-20
Public Version
1
Public Version Date
2023-06-28
Public Version Status
New
Public Device Record Key
02f09c09-57e4-4ed8-b367-eb64ee2688bf

Device Description

Inogen One G3 Replacement Sieve Beds

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
CAW Generator, Oxygen, Portable

GMDN Terms

Code Name
31321 Mobile/portable oxygen concentrator

Identifiers

Type ID
Primary 00867460000120

Customer Contacts

Phone
2487090490

Premarket Submissions

Submission Number Supplement Number
K211056 000