FDA UDI In Commercial Distribution 🇺🇸 United States

MAGNETIC PROBE

DI: 00192896070158 · Model: 2800-7480 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
MAGNETIC PROBE
Primary DI
00192896070158
Version / Model
2800-7480
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-09-07
Public Version
1
Public Version Date
2018-10-08
Public Version Status
New
Public Device Record Key
5f76fd55-132c-4e0f-8110-a22280c0761f

Device Description

HEARTLINE MAGNETIC PROBE

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
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
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
["Dry Heat Sterilization", "Moist Heat or Steam Sterilization"]

Product Codes

Code Name
FGM Probe And Director, Gastro-Urology

GMDN Terms

Code Name
62044 Sharp surgical instrument retrieval magnet

Identifiers

Type ID
Previous B099280074800
Primary 00192896070158

Customer Contacts

Phone
800-821-7496

Device Sizes

Type Value Unit Text
Length 13.75 Inch