LAMBERT KAY AORTIC CLAMP

GUDID B09921007320

Surgical soft-tissue manipulation forceps, scissors-like, reusable

Primary Device ID	B09921007320
NIH Device Record Key	46b4a634-c8ce-48a4-b39f-173cd64c988b
Commercial Distribution Status	In Commercial Distribution
Brand Name	LAMBERT KAY AORTIC CLAMP
Version Model Number	2100-732
Company DUNS	040729840
Company Name	SONTEC INSTRUMENTS, INC.
Device Count	1
DM Exempt	false
Pre-market Exempt	false
MRI Safety Status	Labeling does not contain MRI Safety Information
Human Cell/Tissue Product	false
Device Kit	false
Device Combination Product	false
Single Use	false
Lot Batch	true
Serial Number	false
Manufacturing Date	false
Expiration Date	false
Donation Id Number	false
Contains Natural Rubber Latex	false
Labeled No Natural Rubber Latex	false
RX Perscription	true
OTC Over-The-Counter	false

Device Issuing Agency	Device ID
GS1	00192896003200 [Primary]
HIBCC	B09921007320 [Previous]

DXC	Clamp, Vascular

Steralize Prior To Use	true
Device Is Sterile	false

[B09921007320]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[B09921007320]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

[B09921007320]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

B0992100732L0	LAMBERT KAY AORTIC DEBAKEY CLAMP DOUBLE CURVED JAW ANGLED SHANK
B09921007320	LAMBERT KAY AORTIC DEBAKEY CLAMP DOUBLE CURVED JAW ANGLED SHANK