FDA UDI In Commercial Distribution 🇺🇸 United States

SONTEC DYNAMIC PUNCH

DI: 00192896033320 · Model: 404-3902 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
SONTEC DYNAMIC PUNCH
Primary DI
00192896033320
Version / Model
404-3902
Catalog Number
404-3902
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-09-10
Public Version
1
Public Version Date
2018-10-11
Public Version Status
New
Public Device Record Key
64fe7266-703a-464b-9fe1-7ed4be4ab665

Device Description

SONTEC DYNAMIC PUNCH RONGEUR 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
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
LRY PUNCH, SURGICAL

GMDN Terms

Code Name
35287 Bone punch, reusable

Identifiers

Type ID
Primary 00192896033320

Customer Contacts

Device Sizes

Type Value Unit Text
Length 7 Inch
Device Size Text, specify 30 Degree Tip
Device Size Text, specify 360 Degree Shaft
Device Size Text, specify 2 Millimeter Tip