FDA UDI In Commercial Distribution 🇺🇸 United States

Handheld Pulse Monitor

DI: 06932562310058 · Model: M800 · Guangdong Biolight Meditech Co., Ltd.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Handheld Pulse Monitor
Primary DI
06932562310058
Version / Model
M800
Company Name
Guangdong Biolight Meditech Co., Ltd.
Labeler DUNS
530120146
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-22
Public Version
4
Public Version Date
2021-11-10
Public Version Status
Update
Public Device Record Key
6d85a21b-2d55-446b-8dc4-12f792d8ab17

Device Description

The monitor is indicated for spot checking of functional arterial SpO2(BLT-SpO2), and pulse rate of patient.

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 06932562310058

Premarket Submissions

Submission Number Supplement Number
K101694 000