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AccuMedx

FDA UDI

Class II (US FDA UDI)

by Accumedx, LLC

Identity

Trade Name
AccuMedx FDA UDI
Generic Name
Spring-loaded pneumoperitoneum needle, single-use FDA UDI
Device Name
150 mm Length Stainless Steel Veress Needle FDA UDI
Model / Reference
AMVN-150 FDA UDI
Description
150 mm Length Stainless Steel Veress Needle FDA UDI

Identifiers

Primary DI / UDI-DI
00850059707012 FDA UDI
FDA Product Code
FHO FDA UDI
HIF FDA UDI
GMDN Term
Spring-loaded pneumoperitoneum needle, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1500 FDA UDI
884.1730 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

AccuMedx by Accumedx, LLC — 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
Accumedx, LLC

Sources (1)

  • FDA UDI ba1c1106-c964-4b56-bf5e-197ffa757886 33 fields · synced May 29, 2026