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Medco Manufacturing

FDA UDI

Class II (US FDA UDI)

by Medco Manufacturing LLC

Identity

Trade Name
Medco Manufacturing FDA UDI
Generic Name
Surgical suction system collection container, reusable FDA UDI
Device Name
Large Lid, 6-10mm, for 1000mL, 2000mL and 5000mL Canisters FDA UDI
Model / Reference
MM-L-LG FDA UDI
Description
Large Lid, 6-10mm, for 1000mL, 2000mL and 5000mL Canisters FDA UDI

Identifiers

Primary DI / UDI-DI
00810130454822 FDA UDI
FDA Product Code
KDQ FDA UDI
GMDN Term
Surgical suction system collection container, reusable 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

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Surgical suction system collection container, reusable

Medco Manufacturing by Medco Manufacturing LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical suction system collection container, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 7bd19f80-92c1-4b3b-b88c-06f25e756d7e 34 fields · synced May 29, 2026