← Back to catalogue

Mictec Aspiration Cannula

FDA UDI

Class II (US FDA UDI)

by Sontec Instruments, Inc.

Identity

Trade Name
MICTEC ASPIRATION CANNULA FDA UDI
Generic Name
Body aspiration needle, reusable FDA UDI
Device Name
MICTEC ASPIRATION CANNULA WITH NEEDLE GAUGE 18 FDA UDI
Model / Reference
26941-42 FDA UDI
Description
MICTEC ASPIRATION CANNULA WITH NEEDLE GAUGE 18 FDA UDI

Identifiers

Primary DI / UDI-DI
00192896008984 FDA UDI
510(k) Number
K002877 FDA UDI
FDA Product Code
GCJ FDA UDI
GMDN Term
Body aspiration needle, 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

Dimensions & Sizes

Size
Length — 360 Millimeter FDA UDI

Category: Body aspiration needle, reusable

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

Similar devices

Also classified as Body aspiration needle, reusable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI afc6b7ea-882d-4121-9681-c1b2b311c6ac 36 fields · synced May 30, 2026