RTK10531 OR Turnover Kit RTK10531

GUDID 20787551040337

Operating room turnover kit

Primary Device ID	20787551040337
NIH Device Record Key	c3044208-c537-4da0-be93-a627f2105f58
Commercial Distribution Status	In Commercial Distribution
Brand Name	RTK10531 OR Turnover Kit
Version Model Number	RTK10531
Catalog Number	RTK10531
Company DUNS	868042664
Company Name	XODUS MEDICAL, 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	true
Device Combination Product	false
Single Use	true
Lot Batch	true
Serial Number	true
Manufacturing Date	false
Expiration Date	false
Donation Id Number	false
Contains Natural Rubber Latex	false
Labeled No Natural Rubber Latex	true
RX Perscription	false
OTC Over-The-Counter	false

Device Issuing Agency	Device ID
GS1	00787551040333 [Primary]
GS1	20787551040337 [Package] Contains: 00787551040333 Package: CASE [18 Units] In Commercial Distribution

KDD	Kit, surgical instrument, disposable

Steralize Prior To Use	false
Device Is Sterile	false

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