FDA UDI In Commercial Distribution 🇺🇸 United States

BLUE JAY

DI: 06942820462535 · Model: BJ240105 · Beijing Choice Electronic Technology Co., Ltd.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
BLUE JAY
Primary DI
06942820462535
Version / Model
BJ240105
Company Name
Beijing Choice Electronic Technology Co., Ltd.
Labeler DUNS
526882823
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2026-01-23
Public Version
1
Public Version Date
2026-02-02
Public Version Status
New
Public Device Record Key
27f13a57-47b7-4975-8ffb-8badf1269b4a

Device Description

BLUE JAY FINGER PULSE OXIMETER BJ240105

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
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
45607 Pulse oximeter

Identifiers

Type ID
Primary 06942820462535