A/PA-1550Z

GUDID 10841983103930

PAPER, ECG-1550A, 10 PADS

NIHON KOHDEN AMERICA, INC.

Electrocardiographic recording paper
Primary Device ID10841983103930
NIH Device Record Key816b9156-1c3a-475c-8858-9b8e2bf165d0
Commercial Distribution Discontinuation2023-08-15
Commercial Distribution StatusNot in Commercial Distribution
Version Model NumberA/PA-1550Z
Catalog NumberA/PA-1550Z
Company DUNS021063219
Company NameNIHON KOHDEN AMERICA, INC.
Device Count10
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchfalse
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(800)325-0283
Emailinfo@nkusa.com
Phone+1(800)325-0283
Emailinfo@nkusa.com
Phone+1(800)325-0283
Emailinfo@nkusa.com
Phone+1(800)325-0283
Emailinfo@nkusa.com
Phone+1(800)325-0283
Emailinfo@nkusa.com
Phone+1(800)325-0283
Emailinfo@nkusa.com
Phone+1(800)325-0283
Emailinfo@nkusa.com
Phone+1(800)325-0283
Emailinfo@nkusa.com
Phone+1(800)325-0283
Emailinfo@nkusa.com
Phone+1(800)325-0283
Emailinfo@nkusa.com
Phone+1(800)325-0283
Emailinfo@nkusa.com
Phone+1(800)325-0283
Emailinfo@nkusa.com
Phone+1(800)325-0283
Emailinfo@nkusa.com
Phone+1(800)325-0283
Emailinfo@nkusa.com
Phone+1(800)325-0283
Emailinfo@nkusa.com
Phone+1(800)325-0283
Emailinfo@nkusa.com
Phone+1(800)325-0283
Emailinfo@nkusa.com
Phone+1(800)325-0283
Emailinfo@nkusa.com
Phone+1(800)325-0283
Emailinfo@nkusa.com
Phone+1(800)325-0283
Emailinfo@nkusa.com
Phone+1(800)325-0283
Emailinfo@nkusa.com
Phone+1(800)325-0283
Emailinfo@nkusa.com
Phone+1(800)325-0283
Emailinfo@nkusa.com
Phone+1(800)325-0283
Emailinfo@nkusa.com
Phone+1(800)325-0283
Emailinfo@nkusa.com
Phone+1(800)325-0283
Emailinfo@nkusa.com
Phone+1(800)325-0283
Emailinfo@nkusa.com
Phone+1(800)325-0283
Emailinfo@nkusa.com
Phone+1(800)325-0283
Emailinfo@nkusa.com
Phone+1(800)325-0283
Emailinfo@nkusa.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100841983103933 [Unit of Use]
GS110841983103930 [Primary]

FDA Product Code

DPSELECTROCARDIOGRAPH

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2023-08-17
Device Publish Date2016-09-24

Devices Manufactured by NIHON KOHDEN AMERICA, INC.

10841983103947 - NA2023-10-09 PAPER, ECG1250, 9020, 10 PADS
10841983103954 - NA2023-10-09 PAPER, ECG1350, 9130, 10 PADS
10841983103930 - NA2023-08-17PAPER, ECG-1550A, 10 PADS
10841983103930 - NA2023-08-17 PAPER, ECG-1550A, 10 PADS
00841983104336 - NK-HealthProtect Wireless Surge Solution2021-12-31 Wireless Surge Solution, field deployable ambulatory monitoring of up to 8 patients with pop-up central monitoring
10841983102667 - NA2021-11-10 SpO2 probe Adults, child (from 15 to 50 kg) Finger, disposable
10841983102674 - NA2021-11-10 SpO2 probe Child, infant (from 3 to 15 kg) Toe, disposable
10841983102704 - BluPRO®2021-11-10 SpO2 probe Adults (30 kg or more) Finger or toe, disposable, 80cm cable
10841983102711 - BluPRO®2021-11-10 SpO2 probe Adults (30 kg or more) Finger or toe, disposable, 160cm cable

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.