FDA UDI In Commercial Distribution 🇺🇸 United States

Perforated Sterilizing Inlay

DI: 00192896111578 · Model: 70373-58-062 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Perforated Sterilizing Inlay
Primary DI
00192896111578
Version / Model
70373-58-062
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-11-01
Public Version
2
Public Version Date
2022-09-16
Public Version Status
Update
Public Device Record Key
f927a6ec-a1f6-455b-8ed0-e236541e0588

Device Description

Perforated Sterilizing Inlay for Tray 360 X 230 X 33.5 Millimeter

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
FSM TRAY, SURGICAL, INSTRUMENT

GMDN Terms

Code Name
12143 Instrument tray, reusable

Identifiers

Type ID
Primary 00192896111578

Customer Contacts