FDA UDI In Commercial Distribution 🇺🇸 United States

ST MARKS PERINEAL RETRACTOR BLADES

DI: 00192896044265 · Model: 508-303 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ST MARKS PERINEAL RETRACTOR BLADES
Primary DI
00192896044265
Version / Model
508-303
Catalog Number
508-303
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-09-14
Public Version
2
Public Version Date
2023-02-24
Public Version Status
Update
Public Device Record Key
2d590cb4-1ef0-4209-a590-183653b55929

Device Description

ST MARKS PERINEAL RETRACTOR BLADES (PAIR)

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

Product Codes

Code Name
FFO RETRACTOR, SELF-RETAINING

GMDN Terms

Code Name
46774 Surgical retractor/retraction system blade, reusable

Identifiers

Type ID
Primary 00192896044265

Customer Contacts

Device Sizes

Type Value Unit Text
Length 1.75 Inch