MICASEPT KELLY FORCEPS

GUDID B09920921290

MICASEPT KELLY FORCEPS WITHOUT RATCHET CURVED DOWN

SONTEC INSTRUMENTS, INC.

Rigid endoscopic tissue manipulation forceps, reusable
Primary Device IDB09920921290
NIH Device Record Keyccd4ce0d-1349-4b48-91e5-bbd82063f55b
Commercial Distribution StatusIn Commercial Distribution
Brand NameMICASEPT KELLY FORCEPS
Version Model Number20921-29
Company DUNS040729840
Company NameSONTEC INSTRUMENTS, INC.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone800-821-7496
Emailinfo@sontecinstruments.com
Phone800-821-7496
Emailinfo@sontecinstruments.com
Phone800-821-7496
Emailinfo@sontecinstruments.com

Device Dimensions

Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0

Device Identifiers

Device Issuing AgencyDevice ID
GS100192896008632 [Primary]
HIBCCB09920921290 [Previous]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

GCJLaparoscope, General & Plastic Surgery

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[B09920921290]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[B09920921290]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


[B09920921290]

Dry Heat Sterilization;Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2019-08-21
Device Publish Date2018-08-24

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