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Sun Medical Inc

FDA UDI

Class II (US FDA UDI)

by Sun Medical, Inc.

Identity

Trade Name
Sun Medical Inc FDA UDI
Generic Name
Suction cannula, single-use FDA UDI
Device Name
12mm Straight Cannula FDA UDI
Model / Reference
84112 FDA UDI
Description
12mm Straight Cannula FDA UDI

Identifiers

Catalog Number
84112 FDA UDI
Primary DI / UDI-DI
B226841120 FDA UDI
FDA Product Code
HDB FDA UDI
GMDN Term
Suction cannula, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
884.4340 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

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

Yes

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
Outer Diameter — 12 Millimeter FDA UDI

Category: Suction cannula, single-use

Sun Medical Inc by Sun Medical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Suction cannula, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Sun Medical, Inc.

Sources (1)

  • FDA UDI 12f8dfc6-ee24-47c1-8fc5-589f5207a716 36 fields · synced May 30, 2026