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Blueendo

FDA UDI

Class II (US FDA UDI)

by TROKAMED GmbH

Identity

Trade Name
BLUEENDO FDA UDI
Generic Name
Laparoscopic access cannula, reusable FDA UDI
Device Name
Obturator Ø 20 mm for complete system FDA UDI
Model / Reference
55-201006 FDA UDI
Description
Obturator Ø 20 mm for complete system FDA UDI

Identifiers

Catalog Number
501-040-731 FDA UDI
Primary DI / UDI-DI
04251303822028 FDA UDI
FDA Product Code
HET FDA UDI
GMDN Term
Laparoscopic access cannula, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
884.1720 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

Yes

FDA UDI

Over-the-Counter

Yes

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: Laparoscopic access cannula, reusable

Blueendo by TROKAMED GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Laparoscopic access cannula, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
TROKAMED GmbH

Sources (1)

  • FDA UDI 2bcf2b1c-55e7-4eb9-a85e-fb8539657886 35 fields · synced May 30, 2026