FDA UDI In Commercial Distribution 🇺🇸 United States

BALL POINT PROBE

DI: 00192896070189 · Model: 2800-7486 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
BALL POINT PROBE
Primary DI
00192896070189
Version / Model
2800-7486
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
4f5540b4-fdda-4c93-9ec9-cac8f2ca766f

Device Description

HEARTLINE BALL POINT 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
["Moist Heat or Steam Sterilization", "Dry Heat Sterilization"]

Product Codes

Code Name
FGM Probe And Director, Gastro-Urology

GMDN Terms

Code Name
11268 Vascular dilator, reusable

Identifiers

Type ID
Previous B099280074860
Primary 00192896070189

Customer Contacts

Phone
800-821-7496

Device Sizes

Type Value Unit Text
Length 13.75 Inch