FDA UDI In Commercial Distribution 🇺🇸 United States

Fisher & Paykel Healthcare

DI: 09420012408174 · Model: 200NS003 · FISHER & PAYKEL HEALTHCARE LIMITED
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Fisher & Paykel Healthcare
Primary DI
09420012408174
Version / Model
200NS003
Catalog Number
200NS003
Company Name
FISHER & PAYKEL HEALTHCARE LIMITED
Labeler DUNS
590153276
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-08
Public Version
4
Public Version Date
2021-02-19
Public Version Status
Update
Public Device Record Key
881e9de4-c188-4d93-a912-be84af4ad7d5

Device Description

DUAL ELECTRODES,DISP. (100 PACK)

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
No
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
KOI Stimulator, Nerve, Peripheral, Electric

GMDN Terms

Code Name
35995 Transcutaneous electrical stimulation electrode, single-use

Identifiers

Type ID
Primary 09420012408174

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K924234 000

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
5 – 30 Degrees Celsius