FDA UDI In Commercial Distribution 🇺🇸 United States

SINO-K

DI: 06972820960748 · Model: SP1319 · Shenzhen SINO-K Medical Technology Co.,Ltd
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
SINO-K
Primary DI
06972820960748
Version / Model
SP1319
Company Name
Shenzhen SINO-K Medical Technology Co.,Ltd
Labeler DUNS
554477241
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-02-17
Public Version
1
Public Version Date
2022-02-25
Public Version Status
New
Public Device Record Key
62bac9f4-14e1-4f8c-8746-e9c91cc6dcea

Device Description

Disposable SpO2 Sensor

Device Characteristics

Single Use
Yes
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
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
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
31658 Pulse oximeter probe, single-use

Identifiers

Type ID
Primary 06972820960748

Premarket Submissions

Submission Number Supplement Number
K192608 000