← Back to catalogue

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 irrigation/aspiration cannula, non-illuminating, single-use FDA UDI
Device Name
Rounded Magill Suction 9fg contains 25 units FDA UDI
Model / Reference
S047 FDA UDI
Description
Rounded Magill Suction 9fg contains 25 units FDA UDI

Identifiers

Catalog Number
S047 FDA UDI
Primary DI / UDI-DI
05055299101193 FDA UDI
FDA Product Code
GCX FDA UDI
GMDN Term
Surgical irrigation/aspiration 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

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size
Catheter Gauge — 9 French 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

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

Manufacturer

Sources (1)

  • FDA UDI d5d7635f-fa16-4c5b-94a9-e46601a44bc8 37 fields · synced May 30, 2026