FDA UDI In Commercial Distribution 🇺🇸 United States

Retractor

DI: 00192896104341 · Model: 205-830 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Retractor
Primary DI
00192896104341
Version / Model
205-830
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-09-10
Public Version
1
Public Version Date
2020-09-18
Public Version Status
New
Public Device Record Key
a7e4d8f3-4a03-4a58-86f1-a9f60d678c63

Device Description

Flexible Neck Hook Retractor 3 Blunt Prongs

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 00192896104341

Customer Contacts

Device Sizes

Type Value Unit Text
Length 6 Inch