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Tube For Mictec Spray

FDA UDI

Class II (US FDA UDI)

by Sontec Instruments, Inc.

Identity

Trade Name
TUBE FOR MICTEC SPRAY FDA UDI
Generic Name
ENT powder applicator FDA UDI
Device Name
TUBE FOR MICTEC SPRAY NOZZLE DOUBLE ANGLED FDA UDI
Model / Reference
20943-61 FDA UDI
Description
TUBE FOR MICTEC SPRAY NOZZLE DOUBLE ANGLED FDA UDI

Identifiers

Catalog Number
20943-61 FDA UDI
Primary DI / UDI-DI
00192896008885 FDA UDI
510(k) Number
K002877 FDA UDI
FDA Product Code
HET FDA UDI
GMDN Term
ENT powder applicator FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
884.1720 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: ENT powder applicator

Tube For Mictec Spray by Sontec Instruments, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as ENT powder applicator.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 712b6409-aebd-4fc1-b3ca-882f10ec2e68 36 fields · synced May 31, 2026