FDA UDI In Commercial Distribution 🇺🇸 United States

BAYONET LAMINECTOMY RONGEUR

DI: 00192896101654 · Model: 404-469 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
BAYONET LAMINECTOMY RONGEUR
Primary DI
00192896101654
Version / Model
404-469
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-05-18
Public Version
1
Public Version Date
2020-05-26
Public Version Status
New
Public Device Record Key
dfdec1b9-f383-47f9-9192-8e4d811bb089

Device Description

BAYONET LAMINECTOMY RONGEUR STRAIGHT 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
Yes
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 00192896101654

Customer Contacts

Device Sizes

Type Value Unit Text
Length 6 Inch
Device Size Text, specify 4 x 10 Millimeters Tip