FDA UDI In Commercial Distribution 🇺🇸 United States

SMITH-PETERSON LAMINECTOMY RONGEUR

DI: 00192896027862 · Model: 315-689 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
SMITH-PETERSON LAMINECTOMY RONGEUR
Primary DI
00192896027862
Version / Model
315-689
Catalog Number
315-689
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
2
Public Version Date
2019-07-12
Public Version Status
Update
Public Device Record Key
3b360dfc-1c34-4cd7-b080-f8dbd602c365

Device Description

SMITH-PETERSON LAMINECTOMY RONGEUR STOUT MODEL SLIGHT CURVE JAW

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
HTX RONGEUR

GMDN Terms

Code Name
32853 Orthopaedic joint/limb rongeur

Identifiers

Type ID
Primary 00192896027862

Customer Contacts

Device Sizes

Type Value Unit Text
Length 7.5 Inch
Device Size Text, specify 3 x 16 Millimeter Tip