FEMORAL HEAD DISARTICULATOR KNIFE 1103-211

GUDID 00192896090040

Meniscus knife

Primary Device ID	00192896090040
NIH Device Record Key	a172b5c2-dfe8-42be-a34a-003f48d924cf
Commercial Distribution Status	In Commercial Distribution
Brand Name	FEMORAL HEAD DISARTICULATOR KNIFE
Version Model Number	1103-211
Catalog Number	1103-211
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	false
RX Perscription	true
OTC Over-The-Counter	false

Phone	+1(800) 821-7496
Email	info@sontecinstruments.com

Length

5.5 Inch

Device Issuing Agency	Device ID
GS1	00192896090040 [Primary]

HTS	KNIFE, ORTHOPEDIC

Steralize Prior To Use	true
Device Is Sterile	false

[00192896090040]

Dry Heat Sterilization;Moist Heat or Steam Sterilization

00192896090040	FEMORAL HEAD DISARTICULATOR KNIFE SMALL SIZE CURVED BLADE
00192896090033	FEMORAL HEAD DISARTICULATOR KNIFE LARGE SIZE CURVED BLADE