FDA UDI In Commercial Distribution 🇺🇸 United States

MIKULICZ RETRACTOR

DI: 00192896019751 · Model: 20-0930 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
MIKULICZ RETRACTOR
Primary DI
00192896019751
Version / Model
20-0930
Catalog Number
20-0930
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-09-11
Public Version
2
Public Version Date
2026-03-05
Public Version Status
Update
Public Device Record Key
b92f9602-47a2-41e2-b98d-b0eea5df8f43

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
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
FGN RETRACTOR, NON-SELF-RETAINING

GMDN Terms

Code Name
45918 Hand-held surgical retractor, reusable

Identifiers

Type ID
Primary 00192896019751

Customer Contacts

Device Sizes

Type Value Unit Text
Length 10 Inch
Device Size Text, specify 85 x 35 Millimeter Tip