FDA UDI In Commercial Distribution 🇺🇸 United States

TSUR OPEN RHINOPLASTY RETRACTOR

DI: 00192896054226 · Model: 207-295 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
TSUR OPEN RHINOPLASTY RETRACTOR
Primary DI
00192896054226
Version / Model
207-295
Catalog Number
207-295
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-05-28
Public Version
1
Public Version Date
2019-06-05
Public Version Status
New
Public Device Record Key
014e4761-1aee-4955-9eb3-6ca7dc613f39

Device Description

TSUR OPEN RHINOPLASTY RETRACTOR

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 00192896054226

Customer Contacts

Phone
800-821-7496