Mini Stealth 911003-0001

GUDID 00811714035703

Mini Stealth Probe

RESPONSIVE ORTHOPEDICS LLC

Endoscopic surgical probe Endoscopic surgical probe Endoscopic surgical probe Endoscopic surgical probe Endoscopic surgical probe Endoscopic surgical probe Endoscopic surgical probe Endoscopic surgical probe Endoscopic surgical probe Endoscopic surgical probe Endoscopic surgical probe Endoscopic surgical probe Endoscopic surgical probe Endoscopic surgical probe Endoscopic surgical probe Endoscopic surgical probe Endoscopic surgical probe Endoscopic surgical probe

Primary Device ID	00811714035703
NIH Device Record Key	c5085f13-fc49-4256-8c36-69ef138af4eb
Commercial Distribution Status	In Commercial Distribution
Brand Name	Mini Stealth
Version Model Number	911003-0001
Catalog Number	911003-0001
Company DUNS	002745858
Company Name	RESPONSIVE ORTHOPEDICS LLC
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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00811714035703 [Primary]

FDA Product Code

LXH	Orthopedic Manual Surgical Instrument