FDA UDI In Commercial Distribution 🇺🇸 United States

Viatom

DI: 06934440100676 · Model: Oxiband (Checkme) O2 Pulse Oximeter · Shenzhen Viatom Technology Co., Ltd.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Viatom
Primary DI
06934440100676
Version / Model
Oxiband (Checkme) O2 Pulse Oximeter
Company Name
Shenzhen Viatom Technology Co., Ltd.
Labeler DUNS
421357243
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-07-30
Public Version
2
Public Version Date
2021-11-10
Public Version Status
Update
Public Device Record Key
e6fb1b05-7f9f-48ec-9e95-1a35027e6519

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
MR Unsafe
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
DQA Oximeter

GMDN Terms

Code Name
45607 Pulse oximeter

Identifiers

Type ID
Primary 06934440100676