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Schuco

FDA UDI

Class II (US FDA UDI)

by Allied Medical LLC

Identity

Trade Name
Schuco FDA UDI
Generic Name
Surgical suction system collection container, single-use FDA UDI
Device Name
Disposable Suction Canister FDA UDI
Model / Reference
S1160BS-CS FDA UDI
Description
Disposable Suction Canister FDA UDI

Identifiers

Catalog Number
S1160BS-CS FDA UDI
Primary DI / UDI-DI
00026072011591 FDA UDI
FDA Product Code
KDQ FDA UDI
GMDN Term
Surgical suction system collection container, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.6740 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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Surgical suction system collection container, single-use

Schuco by Allied Medical LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Allied Medical LLC

Sources (1)

  • FDA UDI 716ea47a-385b-4532-a6bb-a5b4294965ba 34 fields · synced Jun 8, 2026