FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 08033695729873 · Model: F6749RUSA · FIAB SPA
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
NA
Primary DI
08033695729873
Version / Model
F6749RUSA
Catalog Number
F6749RUSA
Company Name
FIAB SPA
Labeler DUNS
439770017
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-05-29
Public Version
1
Public Version Date
2020-06-08
Public Version Status
New
Public Device Record Key
68097124-aee0-45a9-9798-b9007c412b32

Device Description

ECG patient cables 10 leads with defibrillator protection, Resistance 10 kOhm, with 4mm plug.

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 08033695729873

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