Centrisol Acid Concentrate

GUDID 00677964082214

MEDIVATORS INC.

Haemodialysis concentrate Haemodialysis concentrate Haemodialysis concentrate Haemodialysis concentrate Haemodialysis concentrate Haemodialysis concentrate Haemodialysis concentrate Haemodialysis concentrate Haemodialysis concentrate Haemodialysis concentrate Haemodialysis concentrate Haemodialysis concentrate Haemodialysis concentrate Haemodialysis concentrate Haemodialysis concentrate Haemodialysis concentrate Haemodialysis concentrate Haemodialysis concentrate Haemodialysis concentrate Haemodialysis concentrate Haemodialysis concentrate Haemodialysis concentrate Haemodialysis concentrate Haemodialysis concentrate Haemodialysis concentrate Haemodialysis concentrate Haemodialysis concentrate Haemodialysis concentrate Haemodialysis concentrate Haemodialysis concentrate Haemodialysis concentrate Haemodialysis concentrate Haemodialysis concentrate Haemodialysis concentrate Haemodialysis concentrate Haemodialysis concentrate Haemodialysis concentrate Haemodialysis concentrate Haemodialysis concentrate Haemodialysis concentrate Haemodialysis concentrate Haemodialysis concentrate Haemodialysis concentrate Haemodialysis concentrate Haemodialysis concentrate Haemodialysis concentrate Haemodialysis concentrate Haemodialysis concentrate Haemodialysis concentrate

• Primary Device ID: 00677964082214
• NIH Device Record Key: 2dbebd50-3fb7-4d98-b6a9-d2f9b111b049
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Centrisol Acid Concentrate
• Version Model Number: SB-353
• Company DUNS: 068199363
• Company Name: MEDIVATORS INC.
• 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: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00677964082214 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K843963

FDA Product Code

• FKQ: System, Dialysate Delivery, Central Multiple Patient

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2018-08-13
• Device Publish Date: 2018-07-13

On-Brand Devices [Centrisol Acid Concentrate]

• 30677964091767: SB-353
• 00677964082214: SB-353
• 00677964056468: SB-164
• 30677964056452: SB-164
• 30677964044367: SB-330
• 00677964044359: SB-342
• 30677964044343: SB-342
• 00677964044335: SB-343
• 00677964044328: SB-344
• 30677964044312: SB-344
• 00677964044304: SB-351
• 30677964044299: SB-351
• 00677964044281: SB-352
• 30677964044275: SB-352
• 00677964006012: SB-152
• 00677964005855: SB-144
• 00677964005794: SB-143
• 00677964005732: SB-142
• 00677964005527: SB-127
• 00677964005367: SB-111
• 30677964000615: SB-152
• 30677964000608: SB-151
• 30677964000592: SB-145
• 30677964000585: SB-144
• 30677964000578: SB-143
• 30677964000561: SB-142
• 30677964000554: SB-140
• 30677964000547: SB-137
• 30677964000530: SB-130
• 30677964000523: SB-129
• 30677964000516: SB-127
• 30677964000509: SB-123
• 30677964000493: SB-119
• 30677964000486: SB-111