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Muc-X

FDA UDI

Class I (US FDA UDI)

by Utah Medical Products, Inc.

Identity

Trade Name
MUC-X FDA UDI
Generic Name
ENT surgical aspirator FDA UDI
Device Name
MUC-X 8FR MUCOUS TRAP W/ WALL UNIT SUCTION ADAPTOR FDA UDI
Model / Reference
8 French FDA UDI
Description
MUC-X 8FR MUCOUS TRAP W/ WALL UNIT SUCTION ADAPTOR FDA UDI

Identifiers

Catalog Number
IM7088FR0 FDA UDI
Primary DI / UDI-DI
H671IM7088FR0 FDA UDI
510(k) Number
K893204 FDA UDI
FDA Product Code
BSY FDA UDI
GMDN Term
ENT surgical aspirator FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.6810 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: ENT surgical aspirator

Muc-X by Utah Medical Products, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as ENT surgical aspirator.

Cleared under the same submission

K893204 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 76b6b918-1a8c-4bb5-989d-e95d0da6592e 36 fields · synced Jun 9, 2026