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MD EndoGuidance Laparoscopic Insufflator

FDA UDI

Class II (US FDA UDI)

by Medical Disposables Corp

Identity

Trade Name
MD EndoGuidance Laparoscopic Insufflator FDA UDI
Generic Name
Spring-loaded pneumoperitoneum needle, single-use FDA UDI
Device Name
Veress Needle 150m Length Stainless Steel Veress Needle FDA UDI
Model / Reference
MDVN-150 FDA UDI
Description
Veress Needle 150m Length Stainless Steel Veress Needle FDA UDI

Identifiers

Primary DI / UDI-DI
00810143450750 FDA UDI
FDA Product Code
HIF FDA UDI
FHO FDA UDI
GMDN Term
Spring-loaded pneumoperitoneum needle, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
884.1730 FDA UDI
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: Spring-loaded pneumoperitoneum needle, single-use

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

Similar devices

Also classified as Spring-loaded pneumoperitoneum needle, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medical Disposables Corp

Sources (1)

  • FDA UDI e7a18aba-f92f-42ab-b737-e55f839ca653 33 fields · synced May 31, 2026