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YelloPort.tif

FDA UDI

Class II (US FDA UDI)

by Surgical Innovations Limited

Identity

Trade Name
YelloPort.tif FDA UDI
Generic Name
Laparoscopic access cannula, reusable FDA UDI
Device Name
LAPAROSCOPIC PORT ACCESS SYSTEM Stopcock Tap Assembly Laparoscopic sleeve - FDA UDI
Model / Reference
Stopcock Tap Assembly FDA UDI
Description
LAPAROSCOPIC PORT ACCESS SYSTEM Stopcock Tap Assembly Laparoscopic sleeve - FDA UDI

Identifiers

Primary DI / UDI-DI
05051986001722 FDA UDI
510(k) Number
K070712 FDA UDI
FDA Product Code
GCJ FDA UDI
GMDN Term
Laparoscopic access cannula, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1500 FDA UDI
Commercial Distribution
Not 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

YelloPort.tif by Surgical Innovations 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

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Manufacturer

Sources (1)

  • FDA UDI 026a59f9-5990-4fda-8637-1521a7674935 35 fields · synced Jun 8, 2026