FDA UDI In Commercial Distribution 🇺🇸 United States

KILLIAN ELEVATOR

DI: 00192896091986 · Model: 412-536 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
KILLIAN ELEVATOR
Primary DI
00192896091986
Version / Model
412-536
Catalog Number
412-536
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-11-22
Public Version
2
Public Version Date
2020-12-04
Public Version Status
Update
Public Device Record Key
83c32da9-d587-4432-a13e-a128d8f6ed4c

Device Description

KILLIAN ELEVATOR DOUBLE ENDED SHARP/BLUNT 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
["Moist Heat or Steam Sterilization", "Dry Heat Sterilization"]

Product Codes

Code Name
HTE ELEVATOR

GMDN Terms

Code Name
38168 Periosteal elevator, reusable

Identifiers

Type ID
Primary 00192896091986

Customer Contacts

Device Sizes

Type Value Unit Text
Length 7.25 Inch