SLOTTED WHISKER

GUDID 04048551110362

Slotted Whisker

Karl Storz GmbH & Co. KG

Arthroscopic shaver system blade, reusable Arthroscopic shaver system blade, reusable Arthroscopic shaver system blade, reusable Arthroscopic shaver system blade, reusable Arthroscopic shaver system blade, reusable Arthroscopic shaver system blade, reusable Arthroscopic shaver system blade, reusable Arthroscopic shaver system blade, reusable Arthroscopic shaver system blade, reusable Arthroscopic shaver system blade, reusable Arthroscopic shaver system blade, reusable Arthroscopic shaver system blade, reusable Arthroscopic shaver system blade, reusable Arthroscopic shaver system blade, reusable Arthroscopic shaver system blade, reusable Arthroscopic shaver system blade, reusable Arthroscopic shaver system blade, reusable Arthroscopic shaver system blade, reusable Arthroscopic shaver system blade, reusable Arthroscopic shaver system blade, reusable Arthroscopic shaver system blade, reusable Arthroscopic shaver system blade, reusable Arthroscopic shaver system blade, reusable

Primary Device ID	04048551110362
NIH Device Record Key	ce2a855a-276b-42fa-9951-5071fd4c3c75
Commercial Distribution Status	In Commercial Distribution
Brand Name	SLOTTED WHISKER
Version Model Number	28205LD
Company DUNS	315731430
Company Name	Karl Storz GmbH & Co. KG
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 Identifiers

Device Issuing Agency	Device ID
GS1	04048551110362 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

Premarket Notification: K030009

FDA Product Code

HRX	ARTHROSCOPE