FDA UDI In Commercial Distribution 🇺🇸 United States

BONE MALLET

DI: 00192896094451 · Model: 330-839 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
BONE MALLET
Primary DI
00192896094451
Version / Model
330-839
Catalog Number
330-839
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-03-07
Public Version
1
Public Version Date
2019-03-15
Public Version Status
New
Public Device Record Key
e0bad34a-af72-4bb1-84bc-0ab907bf225c

Device Description

BONE MALLET AO TYPE PHENOLIC HANDLE

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
HXL MALLET

GMDN Terms

Code Name
32312 Surgical mallet

Identifiers

Type ID
Primary 00192896094451

Customer Contacts

Device Sizes

Type Value Unit Text
Length 9 Inch