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Anivia SG1000 Pump Console

FDA UDI

Class II (US FDA UDI)

by Apmtd, Inc.

Identity

Trade Name
Anivia SG1000 Pump Console FDA UDI
Generic Name
Cardiopulmonary bypass system centrifugal pump drive unit FDA UDI
Device Name
Flow Bubble Sensor FDA UDI
Model / Reference
SG1000-FBS-002 FDA UDI
Description
Flow Bubble Sensor FDA UDI

Identifiers

Catalog Number
SG1000-FBS-002 FDA UDI
Primary DI / UDI-DI
00850000067110 FDA UDI
FDA Product Code
DWA FDA UDI
GMDN Term
Cardiopulmonary bypass system centrifugal pump drive unit FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.4380 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Cardiopulmonary bypass system centrifugal pump drive unit

Anivia SG1000 Pump Console by Apmtd, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Cardiopulmonary bypass system centrifugal pump drive unit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Apmtd, Inc.

Sources (1)

  • FDA UDI 66c401bc-eb2b-48a8-a5da-c546711339f2 36 fields · synced May 30, 2026