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Microsafe

FDA UDI

Class II (US FDA UDI)

by Conmed Corporation

Identity

Trade Name
MICROSAFE FDA UDI
Generic Name
Surgical plume evacuation system filter FDA UDI
Device Name
MicroSafe Smoke Evacuation Filter with 1/4 Inch (6.4mm), 3/8 Inch (9.5mm), and 7/8 Inch (22mm) Ports FDA UDI
Model / Reference
MGVS35302 FDA UDI
Description
MicroSafe Smoke Evacuation Filter with 1/4 Inch (6.4mm), 3/8 Inch (9.5mm), and 7/8 Inch (22mm) Ports FDA UDI

Identifiers

Catalog Number
MGVS35302 FDA UDI
Primary DI / UDI-DI
20845854053123 FDA UDI
510(k) Number
K930041 FDA UDI
FDA Product Code
FYD FDA UDI
GMDN Term
Surgical plume evacuation system filter FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.5070 FDA UDI
Commercial Distribution
Not 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Microsafe by Conmed Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Cleared under the same submission

K930041 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Conmed Corporation

Sources (1)

  • FDA UDI 8b448e89-703b-4944-b1df-61ec0326bad4 37 fields · synced Jun 1, 2026