← Back to catalogue
Endo-Flexprobe
FDA UDIEUDAMEDClass I (US FDA UDI)
Ref TEFP15020
by Joimax, Inc.
Identity
- Trade Name
- Endo-Flexprobe 150 EUDAMEDEndo-Flexprobe FDA UDI
- Generic Name
- Nerve/vessel retractor FDA UDI
- Device Name
- Endo-Flexprobe EUDAMEDEndo-Flexprobe 150 FDA UDI
- Model / Reference
- TEFP15020 EUDAMEDFDA UDI
- Description
- Endo-Flexprobe 150 FDA UDI
Identifiers
- Catalog Number
- TEFP15020 FDA UDI
- Primary DI / UDI-DI
- 04250337120520 EUDAMEDFDA UDI
- Basic UDI-DI
- 42503371PALPENDG5 EUDAMED
- Direct Marketing DI
- 04250337120520 EUDAMED
- FDA Product Code
- GFI FDA UDI
- EMDN Code
- L110599 NEUROSURGERY SPREADERS AND RETRACTORS, REUSABLE - OTHER EUDAMED
- GMDN Term
- Nerve/vessel retractor FDA UDI
Classification
- Device Class
- Class I EUDAMEDFDA UDI
- Regulation Number
- 878.4800 FDA UDI
- Market of Registration
- Germany EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
EUDAMEDFDA UDI
Single Use
No
FDA UDI
Implantable
No
EUDAMEDFDA UDI
Reusable
Yes
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
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Nerve/vessel retractor
Endo-Flexprobe by Joimax, Inc. — Class I — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS
Similar devices
Also classified as Nerve/vessel retractor.
- Ambler Surgical — Ambler Surgical, LLC · Class I
- BOSS Instruments — Boss Instruments, Ltd. · Class I
- Life Instruments — Life Instrument Corporation · Class I
- Medicon — Medicon eG. Chirurgiemechaniker-Genossenschaft · Class I
- JACOBSON SHEPARDS HOOK PROBE — SONTEC INSTRUMENTS, INC. · Class I
- Avalign — AVALIGN TECHNOLOGIES, Inc. · Class I
- Integra® Ruggles®-Redmond™ — Integra LifeSciences Production Corporation · Class I
- RAVINE Lateral Access System — K2M, INC. · 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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Joimax, Inc.
Sources (2)
- FDA UDI aae09465-32a7-40f7-8b93-275957173323 36 fields · synced Jul 31, 2026
- EUDAMED 72c9ce86-8c85-4007-a649-13202e3127fb 61 fields · synced Jul 31, 2026