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Surgimedics®

FDA UDI

Class II (US FDA UDI)

by Coastal Life Technologies, Inc.

Identity

Trade Name
Surgimedics® FDA UDI
Generic Name
Surgical plume evacuation system filter FDA UDI
Device Name
Smoke Evacuation Pre-filter FDA UDI
Model / Reference
901206 FDA UDI
Description
Smoke Evacuation Pre-filter FDA UDI

Identifiers

Primary DI / UDI-DI
00814716020173 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
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

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

Yes

FDA UDI

Category: Surgical plume evacuation system filter

Surgimedics® by Coastal Life Technologies, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical plume evacuation system filter.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 0b3924e4-c667-4f00-8e94-130776cef9b9 33 fields · synced May 30, 2026