FDA UDI In Commercial Distribution 🇺🇸 United States

STELLBRINK RONGEUR

DI: 00192896027435 · Model: 315-566 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
STELLBRINK RONGEUR
Primary DI
00192896027435
Version / Model
315-566
Catalog Number
315-566
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-09-11
Public Version
2
Public Version Date
2019-07-12
Public Version Status
Update
Public Device Record Key
a7f8144c-86f2-423a-8e5f-7e8051af4c28

Device Description

STELLBRINK RONGEUR SLIGHT CURVED 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 00192896027435

Customer Contacts

Device Sizes

Type Value Unit Text
Length 6.5 Inch
Device Size Text, specify 2 x 8 Millimeter Tip