FDA UDI In Commercial Distribution 🇺🇸 United States

KISTLER EAR CARTILAGE RASPATORY

DI: 00192896080164 · Model: 475-618L · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
KISTLER EAR CARTILAGE RASPATORY
Primary DI
00192896080164
Version / Model
475-618L
Catalog Number
475-618L
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
9327a9cb-e865-4f15-a4e6-0fce951d851c

Device Description

KISTLER EAR CARTILAGE RASPATORY LEFT CURVED TIP

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
JYY RASP, EAR

GMDN Terms

Code Name
35295 Middle ear file/rasp

Identifiers

Type ID
Primary 00192896080164

Customer Contacts

Device Sizes

Type Value Unit Text
Length 6.5 Inch