Identity
- Trade Name
- Veress Needle FDA UDI
- Generic Name
- Spring-loaded pneumoperitoneum needle, reusable FDA UDI
- Device Name
- Stainless Steel, 2,00 x 120mm FDA UDI
- Model / Reference
- 1206-20120 FDA UDI
- Description
- Stainless Steel, 2,00 x 120mm FDA UDI
Identifiers
- Catalog Number
- 1206-20120 FDA UDI
- Primary DI / UDI-DI
- 04048223027875 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
- Not 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
Yes
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
No
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Veress Needle by Pajunk GmbH Medizintechnologie — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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 a2e8b778-1c78-4130-965c-93b83318ec05 36 fields · synced Jun 8, 2026