FDA UDI In Commercial Distribution 🇺🇸 United States

ENDOLARYNGEAL PROBE

DI: 00192896058705 · Model: 1301-515 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ENDOLARYNGEAL PROBE
Primary DI
00192896058705
Version / Model
1301-515
Catalog Number
1301-515
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-09-27
Public Version
4
Public Version Date
2024-01-30
Public Version Status
Update
Public Device Record Key
ef745095-afd9-473a-80d3-b92a892c79b7

Device Description

ENDOLARYNGEAL PROBE MICROSCOPIC STRAIGHT BUTTON-END

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
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
KAK PROBE, ENT

GMDN Terms

Code Name
47862 Abdominal/ENT/orthopaedic surgical probe, reusable

Identifiers

Type ID
Primary 00192896058705

Customer Contacts

Device Sizes

Type Value Unit Text
Length 10 Inch