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EndoRetrieval Pouch, 130 × 180 mm
EUDAMEDFDA UDIClass IIa (EU MDR)
Ref PS3443ULTModel TF-1030
Identity
- Trade Name
- EndoRetrieval Pouch, 130 × 180 mm EUDAMEDUltimate Endo Retrieval pouch FDA UDI
- Generic Name
- Tissue extraction bag FDA UDI
- Device Name
- Endoretrieval Pouch EUDAMEDThe Ultimate Endo Retrieval Pouch is used during laparoscopic procedures for retrieving tissue specimens from the abdominal cavity. FDA UDI
- Model / Reference
- TF-1030 EUDAMEDPS3443ULT EUDAMEDFDA UDI
- Description
- The Ultimate Endo Retrieval Pouch is used during laparoscopic procedures for retrieving tissue specimens from the abdominal cavity. FDA UDI
Identifiers
- Catalog Number
- PS3443ULT FDA UDI
- Primary DI / UDI-DI
- 05051223025665 EUDAMEDFDA UDI
- Basic UDI-DI
- B-05051223025665 EUDAMED
- FDA Product Code
- KGY FDA UDI
- EMDN Code
- K01020107 MINIMALLY INVASIVE SURGERY RECOVERY BAGS EUDAMED
- GMDN Term
- Tissue extraction bag FDA UDI
Classification
- Device Class
- Class IIa EUDAMEDClass I FDA UDI
- Regulation Number
- 878.4100 FDA UDI
- Market of Registration
- Spain 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
Dimensions & Sizes
- Size
- Length — 180 Millimeter FDA UDIWidth — 130 Millimeter FDA UDITotal Volume — 580 Milliliter FDA UDI
EndoRetrieval Pouch, 130 × 180 mm by Purple Surgical Holdings Limited also known as Purple Surgical International Limited, Purple Surgical UK Limited and…
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-05051223025665 | 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 95a805be-c08c-41b1-a49f-7bdf9467e121 61 fields · synced Oct 8, 2026
- FDA UDI 39e77e94-c587-47fa-a38b-d928b8eb9d87 36 fields · synced May 30, 2026