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Inflow cannula

FDA UDI

Class II (US FDA UDI)

by SOPRO-COMEG GmbH

Identity

Trade Name
Inflow cannula FDA UDI
Generic Name
Rigid endoscopic cannula, reusable FDA UDI
Model / Reference
191 501 603 FDA UDI

Identifiers

Primary DI / UDI-DI
04059082007830 FDA UDI
510(k) Number
K945263 FDA UDI
FDA Product Code
GCJ FDA UDI
GMDN Term
Rigid endoscopic cannula, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1500 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Rigid endoscopic cannula, reusable

Inflow cannula by SOPRO-COMEG GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Rigid endoscopic cannula, reusable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
SOPRO-COMEG GmbH

Sources (1)

  • FDA UDI 1300a3c2-fcf7-49e3-9dd2-507170a62556 33 fields · synced Jun 6, 2026