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MD EndoGuidance

FDA UDI

Class II (US FDA UDI)

by Medical Disposables Corp

Identity

Trade Name
MD EndoGuidance FDA UDI
Generic Name
Laparoscopic access cannula, single-use FDA UDI
Device Name
Bladeless Trocar 12mm x 150mm FDA UDI
Model / Reference
MD12-150 FDA UDI
Description
Bladeless Trocar 12mm x 150mm FDA UDI

Identifiers

Primary DI / UDI-DI
00810143450187 FDA UDI
FDA Product Code
GCJ FDA UDI
GMDN Term
Laparoscopic access cannula, single-use 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

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Laparoscopic access cannula, single-use

MD EndoGuidance by Medical Disposables Corp — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Laparoscopic access cannula, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI f3e72c02-d9ba-4bef-a0f5-bf82f745cd4e 33 fields · synced May 30, 2026