Identity
- Trade Name
- Veress Needle 120mm EUDAMEDVeress Needle FDA UDI
- Generic Name
- Spring-loaded pneumoperitoneum needle, single-use FDA UDI
- Device Name
- Veress Needle EUDAMEDThe Veress needle is used to establish a pneumoperitoneum prior to abdominal laparoscopic procedures. FDA UDI
- Model / Reference
- TF-1031 EUDAMEDPS3700 EUDAMEDFDA UDI
- Description
- The Veress needle is used to establish a pneumoperitoneum prior to abdominal laparoscopic procedures. FDA UDI
Identifiers
- Catalog Number
- PS3700 FDA UDI
- Primary DI / UDI-DI
- 05051223000792 EUDAMEDFDA UDI
- Basic UDI-DI
- B-05051223000792 EUDAMED
- FDA Product Code
- HET FDA UDI
- EMDN Code
- K0104 VERESS NEEDLES EUDAMED
- GMDN Term
- Spring-loaded pneumoperitoneum needle, single-use FDA UDI
Classification
- Device Class
- Class IIa EUDAMEDClass II FDA UDI
- Regulation Number
- 884.1720 FDA UDI
- Market of Registration
- France EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
EUDAMEDFDA UDI
Single Use
Yes
FDA UDI
Implantable
No
EUDAMEDFDA UDI
Reusable
No
EUDAMED
Contains Latex
No
EUDAMEDFDA UDI
Reprocessed
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
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
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Dimensions & Sizes
- Size
- Length — 120 Millimeter FDA UDI
Veress Needle 120mm by Purple Surgical Holdings Limited also known as Purple Surgical International Limited, Purple Surgical UK Limited and Purple Surgical…
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/MDD
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDD | B-05051223000792 | Class IIa | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class IIa | Pending data |
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Manufacturer
- EUDAMED SRN
- GB-MF-000012819
- Authorised Representative
- Advena Limited MT-AR-000000234
Sources (2)
- EUDAMED 357631dc-42ef-46b0-9312-476670ff747c 61 fields · synced Oct 7, 2026
- FDA UDI 99926fab-3261-479d-b855-6d8f289c60f6 36 fields · synced May 30, 2026