Identity
- Trade Name
- EndoLift EUDAMEDFDA UDI
- Generic Name
- Internally-anchored endoscopic retractor FDA UDI
- Device Name
- EndoLift EUDAMEDThe EndoLift is intended to retract and shift internal organs during minimally invasive surgery. The EndoLift is an internally anchored, hands-free retracting device, which eliminates the need for a hand held retractor during surgery. FDA UDI
- Model / Reference
- EL000A EUDAMEDFDA UDIEL000A5 EUDAMED
- Description
- The EndoLift is intended to retract and shift internal organs during minimally invasive surgery. The EndoLift is an internally anchored, hands-free retracting device, which eliminates the need for a hand held retractor during surgery. FDA UDI
Identifiers
- Catalog Number
- EL000A5 FDA UDI
- Primary DI / UDI-DI
- +M660EL000A51/ EUDAMEDM660EL000A52 FDA UDI
- Basic UDI-DI
- ++M660EL000A5K7 EUDAMED
- Unit of Use DI
- +M660EL000A0Y EUDAMED
- FDA Product Code
- GAD FDA UDI
- EMDN Code
- K01020106,Z12029099 EUDAMED
- GMDN Term
- Internally-anchored endoscopic retractor FDA UDI
Classification
- Device Class
- Class IIa EUDAMEDClass I FDA UDI
- Regulation Number
- 878.4800 FDA UDI
- Market of Registration
- Poland 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
CMR Substance
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Endocrine Disruptor
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
Yes
FDA UDI
Category: Internally-anchored endoscopic retractor
EndoLift by Virtual Ports Ltd — Class I — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS
Similar devices
Also classified as Internally-anchored endoscopic retractor.
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- UpLivt — BOEHRINGER LABORATORIES, LLC · Class II
- Mediflex — ENDOSYS HEALTHCARE INDIA PRIVATE LIMITED · Class I
- ProdiGI — Covidien LP · Class II
- EndoGrab — VIRTUAL PORTS LTD · Class I
- EndoGrab-Short — VIRTUAL PORTS LTD · Class I
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Unknown
MDR
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | MDR | — | Class I | Unknown |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Virtual Ports Ltd
Sources (2)
- FDA UDI e853ba74-315e-494b-82fc-1e333686a4f7 34 fields · synced Jul 21, 2026
- EUDAMED e7953e08-790d-4d2f-97ae-14cac4d148c6 61 fields · synced Jul 21, 2026