FDA UDI In Commercial Distribution 🇺🇸 United States

LUMBAR/CERVICAL IMPACTOR

DI: 00192896031357 · Model: 335-392 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
LUMBAR/CERVICAL IMPACTOR
Primary DI
00192896031357
Version / Model
335-392
Catalog Number
335-392
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-09-12
Public Version
3
Public Version Date
2023-01-20
Public Version Status
Update
Public Device Record Key
d386ec20-0c9b-4f23-9b22-b7ef5d96f757

Device Description

LUMBAR/CERVICAL IMPACTOR MICRO LATERAL OFFSET WITHOUT HEEL

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
HWA IMPACTOR

GMDN Terms

Code Name
32856 Orthopaedic implant impactor, reusable

Identifiers

Type ID
Primary 00192896031357

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify 10 x 4 Millimeter Tip
Length 7 Inch