FDA UDI In Commercial Distribution 🇺🇸 United States

HENLY-CAROTID MENZOIAN RETRACTOR BLADE

DI: 00192896092822 · Model: 230-518-5 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
HENLY-CAROTID MENZOIAN RETRACTOR BLADE
Primary DI
00192896092822
Version / Model
230-518-5
Catalog Number
230-518-5
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-01-04
Public Version
4
Public Version Date
2022-11-01
Public Version Status
Update
Public Device Record Key
bc4d021d-c3a2-4652-b63d-dd771723eb96

Device Description

HENLY-CAROTID MENZOIAN RETRACTOR BLADE EXTRA LONG

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
GAD Retractor

GMDN Terms

Code Name
46774 Surgical retractor/retraction system blade, reusable

Identifiers

Type ID
Primary 00192896092822

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify 0.625 x 1.75 Inches