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Single Use Surgical Professional

FDA UDI

Class II (US FDA UDI)

by Eakin Surgical Limited

Identity

Trade Name
Single Use Surgical Professional FDA UDI
Generic Name
Surgical/emergency suction cannula, non-illuminating, single-use FDA UDI
Device Name
Insulated Suction 6fg 17cm 90 Degrees FDA UDI
Model / Reference
S433 FDA UDI
Description
Insulated Suction 6fg 17cm 90 Degrees FDA UDI

Identifiers

Catalog Number
S433 FDA UDI
Primary DI / UDI-DI
05055299106013 FDA UDI
FDA Product Code
GCX FDA UDI
GMDN Term
Surgical/emergency suction cannula, non-illuminating, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.6740 FDA UDI
Commercial Distribution
Not 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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Angle — 90 degree FDA UDI
Catheter Gauge — 6 French FDA UDI
Length — 17 Centimeter FDA UDI

Single Use Surgical Professional by Eakin Surgical Limited — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Eakin Surgical Limited

Sources (1)

  • FDA UDI 55c2373f-f8a4-459c-b793-fb5f156d94d9 37 fields · synced May 30, 2026