Identity
- Trade Name
- Cutting introducer cannula for Veress- FDA UDI
- Generic Name
- Simple pneumoperitoneum needle FDA UDI
- Device Name
- Cutting introducer cannula for Veress- modular system, 2,00 x 120 mm sterile FDA UDI
- Model / Reference
- 1206-19120 FDA UDI
- Description
- Cutting introducer cannula for Veress- modular system, 2,00 x 120 mm sterile FDA UDI
Identifiers
- Catalog Number
- 1206-19120 FDA UDI
- Primary DI / UDI-DI
- 04048223126257 FDA UDI
- FDA Product Code
- HET FDA UDI
- GMDN Term
- Simple pneumoperitoneum needle 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
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
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
Yes
FDA UDI
Category: Simple pneumoperitoneum needle
Cutting introducer cannula for Veress- by Pajunk GmbH Medizintechnologie — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Simple pneumoperitoneum needle.
- Pneumo-Matic — CooperSurgical, Inc. · Class II
- Pneumo-Matic — CooperSurgical, Inc. · Class II
- Cutting introducer cannula for Veress- — Pajunk GmbH Medizintechnologie · Class II
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Pajunk GmbH Medizintechnologie
Sources (1)
- FDA UDI f16dc49c-a1ed-4034-9c4a-c44a670533bd 36 fields · synced Jun 8, 2026