FDA UDI In Commercial Distribution 🇺🇸 United States

Weil-Blakesley Rongeur

DI: 00192896113114 · Model: 404-771 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Weil-Blakesley Rongeur
Primary DI
00192896113114
Version / Model
404-771
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-07-12
Public Version
1
Public Version Date
2022-07-20
Public Version Status
New
Public Device Record Key
5670997c-fa39-4e76-b64a-9c10be7f2b95

Device Description

Weil-Blakesley Rongeur Fenestrated Jaw Up

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
["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
Primary 00192896113114

Customer Contacts

Device Sizes

Type Value Unit Text
Length 4.5 Inch
Device Size Text, specify Jaw 4 Millimeter