FDA UDI In Commercial Distribution 🇺🇸 United States

UROLOGICAL GYNECOLOGICAL RETRACTOR

DI: 00192896045811 · Model: 520-250 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
UROLOGICAL GYNECOLOGICAL RETRACTOR
Primary DI
00192896045811
Version / Model
520-250
Catalog Number
520-250
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-10-04
Public Version
3
Public Version Date
2021-05-10
Public Version Status
Update
Public Device Record Key
6b8af606-18b4-467d-bcf6-f1a17e7edfb5

Device Description

UROLOGICAL GYNECOLOGICAL RETRACTOR SLING SPACER ANGLED SHAFT

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
HDL RETRACTOR, VAGINAL

GMDN Terms

Code Name
46774 Surgical retractor/retraction system blade, reusable

Identifiers

Type ID
Primary 00192896045811

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify 10 x 90 Millimeter Blades
Device Size Text, specify 45 Degree Blades