FDA UDI In Commercial Distribution 🇺🇸 United States

Fisher & Paykel Healthcare

DI: 09420012433978 · Model: ST520 · FISHER & PAYKEL HEALTHCARE LIMITED
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Fisher & Paykel Healthcare
Primary DI
09420012433978
Version / Model
ST520
Catalog Number
ST520
Company Name
FISHER & PAYKEL HEALTHCARE LIMITED
Labeler DUNS
590153276
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-07-06
Public Version
1
Public Version Date
2023-07-14
Public Version Status
New
Public Device Record Key
6b6bd712-4f73-46ab-a290-50893217cfed

Device Description

HUMIDIFIED INSUFFLATION KIT

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
Yes
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
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
HIF Insufflator, Laparoscopic

GMDN Terms

Code Name
38559 Insufflation gas conditioning tubing set

Identifiers

Type ID
Package 09420012433985
Primary 09420012433978

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K162582 000