PENNINGTON CLAMP INSERT

GUDID B0992901278L0

PENNINGTON CLAMP DOUBLE-ACTION JAWS FOR TUBE SHAFT

SONTEC INSTRUMENTS, INC.

Vascular Doppler clamp
Primary Device IDB0992901278L0
NIH Device Record Key657240de-00e7-4a31-a056-37710586c1a3
Commercial Distribution Discontinuation2018-06-22
Commercial Distribution StatusNot in Commercial Distribution
Brand NamePENNINGTON CLAMP INSERT
Version Model Number2901-278L
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

Device Dimensions

Length450 Millimeter
Device Size Text, specify0
Length450 Millimeter
Device Size Text, specify0

Device Identifiers

Device Issuing AgencyDevice ID
HIBCCB0992901278L0 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

GEIElectrosurgical, Cutting & Coagulation & Accessories

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[B0992901278L0]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[B0992901278L0]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number6
Public Version Date2018-07-06
Device Publish Date2016-08-19

On-Brand Devices [PENNINGTON CLAMP INSERT ]

B0992901278S0PENNINGTON CLAMP DOUBLE-ACTION JAWS FOR TUBE SHAFT
B0992901278L0PENNINGTON CLAMP DOUBLE-ACTION JAWS FOR TUBE SHAFT
B09929012780PENNINGTON CLAMP DOUBLE-ACTION JAWS FOR TUBE SHAFT

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.