FDA UDI In Commercial Distribution 🇺🇸 United States

SONTEC-WECK TROUTMAN CORNEAL DISSECTOR

DI: 00192896072374 · Model: 11-3423 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
SONTEC-WECK TROUTMAN CORNEAL DISSECTOR
Primary DI
00192896072374
Version / Model
11-3423
Catalog Number
11-3423
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-10-08
Public Version
3
Public Version Date
2020-02-24
Public Version Status
Update
Public Device Record Key
bf0a2891-0305-451e-817d-bd1a534d3f1b

Device Description

SONTEC-WECK TROUTMAN CORNEAL DISSECTOR SINGLE ENDED BLADE

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
GDI Dissector, Surgical, General & Plastic Surgery

GMDN Terms

Code Name
32754 Ocular hook/spatula/manipulator, reusable

Identifiers

Type ID
Primary 00192896072374

Customer Contacts

Phone
800-821-7496