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autoLog IQ™

FDA UDI

Class II (US FDA UDI)

by Medtronic, Inc.

Identity

Trade Name
autoLog IQ™ FDA UDI
Generic Name
Autotransfusion system blood collection/processing pump FDA UDI
Device Name
SYSTEM ATLGIQ AUTOTRANSFUSION US FDA UDI
Model / Reference
ATLGIQ FDA UDI
Description
SYSTEM ATLGIQ AUTOTRANSFUSION US FDA UDI

Identifiers

Primary DI / UDI-DI
00643169982864 FDA UDI
510(k) Number
K181954 FDA UDI
FDA Product Code
CAC FDA UDI
GMDN Term
Autotransfusion system blood collection/processing pump FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5830 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

No

FDA UDI

Category: Autotransfusion system blood collection/processing pump

autoLog IQ™ by Medtronic, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Autotransfusion system blood collection/processing pump.

Cleared under the same submission

K181954 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medtronic, Inc.

Sources (1)

  • FDA UDI cf3522ff-f93a-4750-8d18-34f582d13387 36 fields · synced May 30, 2026