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Veress

FDA UDI

Class II (US FDA UDI)

by Pajunk GmbH Medizintechnologie

Identity

Trade Name
VERESS FDA UDI
Generic Name
Spring-loaded pneumoperitoneum needle, reusable FDA UDI
Device Name
1206-21120 FDA UDI
Model / Reference
1206-21120 FDA UDI
Description
1206-21120 FDA UDI

Identifiers

Catalog Number
1206-21120 FDA UDI
Primary DI / UDI-DI
04048223077696 FDA UDI
FDA Product Code
HET FDA UDI
GMDN Term
Spring-loaded pneumoperitoneum needle, 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

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Spring-loaded pneumoperitoneum needle, reusable

Veress by Pajunk GmbH Medizintechnologie — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Spring-loaded pneumoperitoneum needle, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Pajunk GmbH Medizintechnologie

Sources (1)

  • FDA UDI 99699590-1e76-44b6-abd7-3d9faff767f8 36 fields · synced Jun 6, 2026