FDA UDI In Commercial Distribution 🇺🇸 United States

BluPRO®

DI: 04931921877494 · Model: TL-631T3 · NIHON KOHDEN CORPORATION
Product Codes
5
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
BluPRO®
Primary DI
04931921877494
Version / Model
TL-631T3
Catalog Number
TL-631T3
Company Name
NIHON KOHDEN CORPORATION
Labeler DUNS
690568050
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
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
05d4af04-1601-4322-bc40-e1682ad1bb59

Device Description

Finger probe Adult, child (20 kg or more) Finger or toe

Device Characteristics

Single Use
No
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
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

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

GMDN Terms

Code Name
37808 Pulse oximeter probe, reusable

Identifiers

Type ID
Primary 04931921877494

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify Adult