FDA UDI In Commercial Distribution 🇺🇸 United States

THERMOBIO

DI: 06951740540377 · Model: https://gudid.fda.gov/gudid/resources/images/icons/icon_info_small.png · Shenzhen Jumper Medical Equipment Co.,Ltd.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
THERMOBIO
Primary DI
06951740540377
Version / Model
https://gudid.fda.gov/gudid/resources/images/icons/icon_info_small.png
Company Name
Shenzhen Jumper Medical Equipment Co.,Ltd.
Labeler DUNS
529217911
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-10-18
Public Version
1
Public Version Date
2025-10-27
Public Version Status
New
Public Device Record Key
cdd02153-c2ae-4051-b0b5-5fba816c672c

Device Description

Pulse Oximeter

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
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
Yes
Has Serial Number
Yes
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
OCH Oximeter, Infrared, Sporting, Aviation

GMDN Terms

Code Name
45607 Pulse oximeter

Identifiers

Type ID
Primary 06951740540377