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Disposable Cannula Soft Tip Wi

FDA UDI

Class I (US FDA UDI)

by Fci S A S Fci 20 22

Identity

Trade Name
Disposable Cannula Soft Tip Wi FDA UDI
Generic Name
Vitrectomy fluid/gas handling handpiece/cannula FDA UDI
Device Name
Disposable Cannula Soft Tip Wi FDA UDI
Model / Reference
S9.4110.27 FDA UDI
Description
Disposable Cannula Soft Tip Wi FDA UDI

Identifiers

Primary DI / UDI-DI
13700773706980 FDA UDI
FDA Product Code
HMX FDA UDI
GMDN Term
Vitrectomy fluid/gas handling handpiece/cannula FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
886.4350 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

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

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Vitrectomy fluid/gas handling handpiece/cannula

Disposable Cannula Soft Tip Wi by Fci S A S Fci 20 22 — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Vitrectomy fluid/gas handling handpiece/cannula.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Fci S A S Fci 20 22

Sources (1)

  • FDA UDI ac31bdd1-934e-43c5-887a-ad5a0272ac09 33 fields · synced May 30, 2026