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Mictec Spray Nozzle

FDA UDI

Class II (US FDA UDI)

by Sontec Instruments, Inc.

Identity

Trade Name
MICTEC SPRAY NOZZLE FDA UDI
Generic Name
Surgical suction system collection container, reusable FDA UDI
Device Name
MICTEC SPARY NOZZLE WITH BELLOWS-DISC FDA UDI
Model / Reference
20943-50 FDA UDI
Description
MICTEC SPARY NOZZLE WITH BELLOWS-DISC FDA UDI

Identifiers

Catalog Number
20943-50 FDA UDI
Primary DI / UDI-DI
00192896093157 FDA UDI
510(k) Number
K002877 FDA UDI
FDA Product Code
GCJ FDA UDI
GMDN Term
Surgical suction system collection container, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1500 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: Surgical suction system collection container, reusable

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

Similar devices

Also classified as Surgical suction system collection container, reusable.

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 52166d01-1051-4c89-a2d0-ffa472f306fb 36 fields · synced May 30, 2026