FDA UDI In Commercial Distribution 🇺🇸 United States

MIKULICZ RETRACTOR

DI: 00192896100770 · Model: 20-0933 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
MIKULICZ RETRACTOR
Primary DI
00192896100770
Version / Model
20-0933
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-02-24
Public Version
1
Public Version Date
2020-03-03
Public Version Status
New
Public Device Record Key
125220b8-a65c-44a7-be41-65e08f9c6d00

Device Description

MIKULICZ RETRACTOR

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
FGN RETRACTOR, NON-SELF-RETAINING

GMDN Terms

Code Name
45918 Hand-held surgical retractor, reusable

Identifiers

Type ID
Primary 00192896100770

Customer Contacts

Device Sizes

Type Value Unit Text
Length 10.25 Inch
Device Size Text, specify 155 x 50 Millimeter