Barr Probe 508-548

GUDID 00192896122826

Gastro-urological director

Primary Device ID	00192896122826
NIH Device Record Key	228cc917-40cf-4874-920c-a60bb65757c6
Commercial Distribution Status	In Commercial Distribution
Brand Name	Barr Probe
Version Model Number	508-548
Catalog Number	508-548
Company DUNS	040729840
Company Name	SONTEC INSTRUMENTS, INC.
Device Count	1
DM Exempt	false
Pre-market Exempt	true
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	true
RX Perscription	true
OTC Over-The-Counter	false

Device Issuing Agency	Device ID
GS1	00192896122826 [Primary]

FGM	PROBE AND DIRECTOR, GASTRO-UROLOGY

Steralize Prior To Use	true
Device Is Sterile	false

[00192896122826]

Dry Heat Sterilization

[00192896122826]

Dry Heat Sterilization

[00192896122826]

Dry Heat Sterilization

[00192896122826]

Dry Heat Sterilization

[00192896122826]

Dry Heat Sterilization

[00192896122826]

Dry Heat Sterilization

[00192896122826]

Dry Heat Sterilization

00192896044661	BARR PROBE DOUBLE ENDED
00192896122826	Barr Probe Double Ended Tips