FDA UDI In Commercial Distribution 🇺🇸 United States

St. Marks Hand Retractor

DI: 00192896110397 · Model: 508-323BL · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
St. Marks Hand Retractor
Primary DI
00192896110397
Version / Model
508-323BL
Catalog Number
508-323BL
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-06-18
Public Version
2
Public Version Date
2023-06-22
Public Version Status
Update
Public Device Record Key
13957ba6-3c51-4e31-af5c-d2c4f223ac77

Device Description

St. Marks Hand Retractor With Lip 15 Degree Angled Tip Illuminated

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
["Moist Heat or Steam Sterilization", "Dry Heat Sterilization"]

Product Codes

Code Name
FDG Retractor, Fiberoptic

GMDN Terms

Code Name
45918 Hand-held surgical retractor, reusable

Identifiers

Type ID
Primary 00192896110397

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify Blade Length 7 Inches