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Canister Set

FDA UDI

Class II (US FDA UDI)

by Stryker Corp.

Identity

Trade Name
Canister Set FDA UDI
Generic Name
Surgical suction system collection container, single-use FDA UDI
Device Name
Canister Set FDA UDI
Model / Reference
INC-11790 FDA UDI
Description
Canister Set FDA UDI

Identifiers

Catalog Number
INC-11790 FDA UDI
Primary DI / UDI-DI
07613327459289 FDA UDI
510(k) Number
K172167 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

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: Surgical suction system collection container, single-use

Canister Set by Stryker Corp. — 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

K172167 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Stryker Corp.

Sources (1)

  • FDA UDI 20f199e9-326c-428e-b9b2-31fcae54fbd1 37 fields · synced Jun 8, 2026