FDA UDI In Commercial Distribution 🇺🇸 United States

St. Marks Hand Retractor

DI: 00192896109841 · Model: 508-326SL · 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
00192896109841
Version / Model
508-326SL
Catalog Number
508-326SL
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-05-20
Public Version
2
Public Version Date
2023-06-22
Public Version Status
Update
Public Device Record Key
6adc6262-4a6d-443d-8700-3741aade41d8

Device Description

St. Marks Hand Retractor With Lip 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 00192896109841

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify Blade Length 9 Inch