FDA UDI In Commercial Distribution 🇺🇸 United States

FOMON RASP

DI: 00192896078345 · Model: 345-282 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
FOMON RASP
Primary DI
00192896078345
Version / Model
345-282
Catalog Number
345-282
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-09-20
Public Version
2
Public Version Date
2018-12-07
Public Version Status
Update
Public Device Record Key
63184856-427f-4931-9468-1288fefd6e8a

Device Description

FOMON RASP DOUBLE ENDED SINGLE SIDED TUNGSTEN CARBIDE INSERT

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
["Moist Heat or Steam Sterilization", "Dry Heat Sterilization"]

Product Codes

Code Name
KBA RASP, NASAL

GMDN Terms

Code Name
35296 Nasal file/rasp

Identifiers

Type ID
Primary 00192896078345

Customer Contacts

Device Sizes

Type Value Unit Text
Length 8.5 Inch