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Vc-701

FDA UDI

Class II (US FDA UDI)

by Stryker Corp.

Identity

Trade Name
VC-701 FDA UDI
Generic Name
General-purpose surgical suction system, electric FDA UDI
Device Name
Cliq Aspirator FDA UDI
Model / Reference
INC-11648 FDA UDI
Description
Cliq Aspirator FDA UDI

Identifiers

Catalog Number
INC-11648 FDA UDI
Primary DI / UDI-DI
07613327459296 FDA UDI
510(k) Number
K172167 FDA UDI
FDA Product Code
NRY FDA UDI
GMDN Term
General-purpose surgical suction system, electric 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

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: General-purpose surgical suction system, electric

Vc-701 by Stryker Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General-purpose surgical suction system, electric.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Stryker Corp.

Sources (1)

  • FDA UDI 97e1a97c-c859-4461-b31b-f2b19216e287 37 fields · synced May 30, 2026