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Instrumentarium

FDA UDI

Class I (US FDA UDI)

by Société Chirurgicale Instrumentarium Inc

Identity

Trade Name
Instrumentarium FDA UDI
Generic Name
Paranasal sinus irrigation/aspiration cannula FDA UDI
Model / Reference
s.50.775 FDA UDI

Identifiers

Primary DI / UDI-DI
00810055472253 FDA UDI
FDA Product Code
KAM FDA UDI
GMDN Term
Paranasal sinus irrigation/aspiration cannula FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Paranasal sinus irrigation/aspiration cannula

Instrumentarium by Société Chirurgicale Instrumentarium Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Paranasal sinus irrigation/aspiration cannula.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Société Chirurgicale Instrumentarium Inc

Sources (1)

  • FDA UDI 6f91b3b9-5cd3-404a-b107-f878a123bb02 32 fields · synced May 30, 2026