0212-011-000

GUDID 34546540184796

Whole-blood-recovery autotransfusion system, powered

Primary Device ID	34546540184796
NIH Device Record Key	c352ae12-e8c3-4d87-916b-7cf0f016d6f9
Commercial Distribution Discontinuation	2019-03-31
Commercial Distribution Status	Not in Commercial Distribution
Version Model Number	0212011000
Catalog Number	0212-011-000
Company DUNS	196548481
Company Name	STRYKER CORPORATION
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	true
Lot Batch	true
Serial Number	false
Manufacturing Date	false
Expiration Date	true
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)253-3210
Email	Inst.Stryker.cs@Stryker.com

Width

10 Millimeter

Device Issuing Agency	Device ID
GS1	04546540184795 [Primary]
GS1	34546540184796 [Package] Contains: 04546540184795 Package: pack [10 Units] Discontinued: 2019-03-31 Not in Commercial Distribution

CAC	APPARATUS, AUTOTRANSFUSION

Steralize Prior To Use	false
Device Is Sterile	true