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Rico Suction Labs, Inc.

FDA UDI

Class II (US FDA UDI)

by Rico Suction Labs Inc

Identity

Trade Name
Rico Suction Labs, Inc. FDA UDI
Generic Name
Surgical suction system FDA UDI
Device Name
Aspirator FDA UDI
Model / Reference
1001D FDA UDI
Description
Aspirator FDA UDI

Identifiers

Primary DI / UDI-DI
00863110000434 FDA UDI
FDA Product Code
GCX FDA UDI
GMDN Term
Surgical suction system 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

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

Rico Suction Labs, Inc. by Rico Suction Labs Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical suction system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 00d1ae15-0b9a-40e3-b75e-f8357677ff3c 34 fields · synced Jun 1, 2026