FDA UDI In Commercial Distribution 🇺🇸 United States

MICASEPT DUVAL LUNG GRASPER

DI: 00192896010932 · Model: 20919-02-004 · SONTEC INSTRUMENTS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
MICASEPT DUVAL LUNG GRASPER
Primary DI
00192896010932
Version / Model
20919-02-004
Catalog Number
20919-02-004
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
1
Public Version Date
2018-09-17
Public Version Status
New
Public Device Record Key
05922d91-ae34-4522-b948-2c5a0cf9cd4c

Device Description

MICASEPT DUVAL LUNG GRASPER WITH HEGAR RATCHET

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
["Moist Heat or Steam Sterilization", "Dry Heat Sterilization"]

Product Codes

Code Name
GCJ Laparoscope, General & Plastic Surgery

GMDN Terms

Code Name
38661 Rigid endoscopic grasping forceps, reusable

Identifiers

Type ID
Primary 00192896010932

Customer Contacts

Phone
800-821-7496

Premarket Submissions

Submission Number Supplement Number
K002877 000