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Riptide™

FDA UDI

Class II (US FDA UDI)

by Micro Therapeutics, Inc.

Identity

Trade Name
Riptide™ FDA UDI
Generic Name
Surgical suction system collection container, single-use FDA UDI
Device Name
CANISTER MAC-1200 V01 US FDA UDI
Model / Reference
MAC-1200 FDA UDI
Description
CANISTER MAC-1200 V01 US FDA UDI

Identifiers

Primary DI / UDI-DI
00847536029095 FDA UDI
510(k) Number
K172448 FDA UDI
FDA Product Code
NRY FDA UDI
GMDN Term
Surgical suction system collection container, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1250 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Surgical suction system collection container, single-use

Riptide™ by Micro Therapeutics, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical suction system collection container, single-use.

Cleared under the same submission

K172448 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Micro Therapeutics, Inc.

Sources (1)

  • FDA UDI 6b57d224-d97b-47ba-846b-da8dbdcc0241 36 fields · synced May 30, 2026