FDA UDI In Commercial Distribution 🇺🇸 United States

LEKSELL RONGEUR

DI: 00192896096158 · Model: 1100-549 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
LEKSELL RONGEUR
Primary DI
00192896096158
Version / Model
1100-549
Catalog Number
1100-549
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-05-09
Public Version
2
Public Version Date
2019-07-12
Public Version Status
Update
Public Device Record Key
f6484a95-d108-4c29-aaf1-f769ad9296a1

Device Description

LEKSELL RONGEUR LIGHT CURVED 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 00192896096158

Customer Contacts

Phone
800-821-7496

Device Sizes

Type Value Unit Text
Length 15.75 Inch
Device Size Text, specify 5 Millimeter Tip