FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 08033695726360 · Model: F6738RAHA · FIAB SPA
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
NA
Primary DI
08033695726360
Version / Model
F6738RAHA
Catalog Number
F6738RAHA
Company Name
FIAB SPA
Labeler DUNS
439770017
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-09-16
Public Version
1
Public Version Date
2024-09-24
Public Version Status
New
Public Device Record Key
8d5d9259-c84d-4b18-855f-9c13e52a5898

Device Description

ECG patient cables USA version

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
Yes
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
IKD Cable, Electrode

GMDN Terms

Code Name
31683 Electrocardiographic lead switching adaptor

Identifiers

Type ID
Primary 08033695726360

Customer Contacts

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
0 – 50 Degrees Celsius
Type
Storage Environment Humidity
Temperature Range
20 – 80 Percent (%) Relative Humidity