FDA UDI In Commercial Distribution 🇺🇸 United States

THORACOSCOPIC DELUXE SET

DI: 00192896010918 · Model: 20906-2615 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
THORACOSCOPIC DELUXE SET
Primary DI
00192896010918
Version / Model
20906-2615
Catalog Number
20906-2615
Company Name
SONTEC INSTRUMENTS, INC.
Labeler DUNS
040729840
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-08-15
Public Version
2
Public Version Date
2022-06-17
Public Version Status
Update
Public Device Record Key
4611e6ef-9867-4466-b798-788d3b54009a

Device Description

THORACOSCOPIC DELUXE SET

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
No
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
GCJ Laparoscope, General & Plastic Surgery

GMDN Terms

Code Name
44058 General surgical procedure kit, non-medicated, reusable

Identifiers

Type ID
Primary 00192896010918

Customer Contacts

Phone
800-821-7496

Premarket Submissions

Submission Number Supplement Number
K002877 000