FDA UDI In Commercial Distribution 🇺🇸 United States

BluPRO®

DI: 14931921878535 · Model: TL-271T3 · NIHON KOHDEN CORPORATION
Product Codes
4
GMDN Terms
1
Identifiers
2
Pkg Device Count
24

Basic Information

Brand Name
BluPRO®
Primary DI
14931921878535
Version / Model
TL-271T3
Catalog Number
TL-271T3
Company Name
NIHON KOHDEN CORPORATION
Labeler DUNS
690568050
Distribution Status
In Commercial Distribution
Device Count in Pkg
24
Record Status
Published
Publish Date
2016-09-05
Public Version
3
Public Version Date
2021-11-10
Public Version Status
Update
Public Device Record Key
94d2eee8-af89-43e4-af73-6a0d053441b4

Device Description

SpO2 probe Adults (30 kg or more) Finger or toe, disposable

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
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
MHX MONITOR, PHYSIOLOGICAL, PATIENT(WITH ARRHYTHMIA DETECTION OR ALARMS)
DRG TRANSMITTERS AND RECEIVERS, PHYSIOLOGICAL SIGNAL, RADIOFREQUENCY
DRT MONITOR, CARDIAC (INCL. CARDIOTACHOMETER & RATE ALARM)
GWQ Full-montage Standard Electroencephalograph

GMDN Terms

Code Name
31658 Pulse oximeter probe, single-use

Identifiers

Type ID
Primary 14931921878535
Unit of Use 04931921878538

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify Adult