← Back to catalogue
Insufflation Filter/Tubing Set with Push Fit Funnel Connector
EUDAMEDFDA UDIClass IIa (EU MDR)
Ref PS3602Model TF-1025
Identity
- Trade Name
- Insufflation Filter/Tubing Set with Push Fit Funnel Connector EUDAMEDInsufflation filter / tubing set with push fit funnel connector FDA UDI
- Generic Name
- Microbial medical gas filter, sterile, single-use FDA UDI
- Device Name
- Insufflation Filter/Tubing Set EUDAMEDThe Insufflation filter / tubing set effectively prevents cross contamination between the patient & insufflator. FDA UDI
- Model / Reference
- TF-1025 EUDAMEDPS3602 EUDAMEDFDA UDI
- Description
- The Insufflation filter / tubing set effectively prevents cross contamination between the patient & insufflator. FDA UDI
Identifiers
- Catalog Number
- PS3602 FDA UDI
- Primary DI / UDI-DI
- 05051223004097 EUDAMEDFDA UDI
- Basic UDI-DI
- B-05051223004097 EUDAMED
- FDA Product Code
- NKC FDA UDI
- EMDN Code
- K0199 ENDOTHERAPY DEVICES - OTHER EUDAMED
- GMDN Term
- Microbial medical gas filter, sterile, single-use FDA UDI
Classification
- Device Class
- Class IIa EUDAMEDClass I FDA UDI
- Regulation Number
- 884.1730 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
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Insufflation Filter/Tubing Set with Push Fit Funnel Connector by Purple Surgical Holdings Limited also known as Purple Surgical International Limited, Purple…
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-05051223004097 | Class IIa | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class IIa | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- EUDAMED SRN
- GB-MF-000012819
- Authorised Representative
- Advena Limited MT-AR-000000234
Sources (2)
- EUDAMED dde06c8f-dd42-4028-a09b-fd2d8ba65ce2 61 fields · synced Jun 18, 2026
- FDA UDI 20487bb5-7b18-4a8b-8799-47ff68ae6f3c 35 fields · synced May 30, 2026