FDA UDI In Commercial Distribution 🇺🇸 United States

BAILEY AORTIC VALVE RONGEUR

DI: 00192896038523 · Model: 440-313 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
BAILEY AORTIC VALVE RONGEUR
Primary DI
00192896038523
Version / Model
440-313
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-09-06
Public Version
2
Public Version Date
2019-07-12
Public Version Status
Update
Public Device Record Key
41675537-7d7d-4681-a54f-0998b129e852

Device Description

BAILEY RONGEUR

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
No
Has Serial Number
No
Has Lot/Batch Number
No
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
HTX Rongeur

GMDN Terms

Code Name
32853 Orthopaedic joint/limb rongeur

Identifiers

Type ID
Previous B0994403130
Primary 00192896038523

Customer Contacts

Phone
8008217496

Premarket Submissions

Submission Number Supplement Number
K092544 000

Device Sizes

Type Value Unit Text
Length 4.5 Inch