FDA UDI In Commercial Distribution 🇺🇸 United States

SONTEC-CROCK RETRACTOR

DI: 00192896092877 · Model: 417-200 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
SONTEC-CROCK RETRACTOR
Primary DI
00192896092877
Version / Model
417-200
Catalog Number
417-200
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-01-03
Public Version
4
Public Version Date
2023-03-08
Public Version Status
Update
Public Device Record Key
01c7267e-3ae0-43ae-b368-9de05d01645f

Device Description

SONTEC-CROCK RETRACTOR SMALL SIZE

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
GAD Retractor

GMDN Terms

Code Name
45918 Hand-held surgical retractor, reusable

Identifiers

Type ID
Primary 00192896092877

Customer Contacts

Device Sizes

Type Value Unit Text
Length 17.5 Inch