Lateral Disc Prep 112-052

GUDID 00190837089603

Surgical retraction system, reusable

Primary Device ID	00190837089603
NIH Device Record Key	9b01d6dc-ede4-4b1a-941b-3f6a21b06a72
Commercial Distribution Status	In Commercial Distribution
Brand Name	Lateral Disc Prep
Version Model Number	112-052
Catalog Number	112-052
Company DUNS	183641617
Company Name	Life Spine, 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

Device Issuing Agency	Device ID
GS1	00190837089603 [Primary]

LXH	ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

Steralize Prior To Use	true
Device Is Sterile	false

[00190837089603]

Moist Heat or Steam Sterilization