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Endoscope shaft
FDA UDIEUDAMEDClass II (US FDA UDI)
Ref BSHS04175
by Joimax, Inc.
Identity
- Trade Name
- Endoscope shaft with standard lip EUDAMEDEndoscope shaft FDA UDI
- Generic Name
- Endoscope sheath, reusable FDA UDI
- Device Name
- Arthroscope Shaft EUDAMEDEndoscope shaft with standard lip FDA UDI
- Model / Reference
- BSHS04175 EUDAMEDFDA UDI
- Description
- Endoscope shaft with standard lip FDA UDI
Identifiers
- Catalog Number
- BSHS04175 FDA UDI
- Primary DI / UDI-DI
- 04250337120339 EUDAMEDFDA UDI
- Basic UDI-DI
- 42503371ENSCASBW EUDAMED
- Direct Marketing DI
- 04250337120339 EUDAMED
- FDA Product Code
- HRX FDA UDI
- EMDN Code
- L1199 NEUROSURGERY INSTRUMENTS, REUSABLE - OTHER EUDAMED
- GMDN Term
- Endoscope sheath, reusable FDA UDI
Classification
- Device Class
- Class I EUDAMEDClass II FDA UDI
- Regulation Number
- 888.1100 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: Endoscope sheath, reusable
Endoscope shaft by Joimax, Inc. — Class II — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS
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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 II | Unknown |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Joimax, Inc.
Sources (2)
- FDA UDI 653bac73-2c39-4535-a07a-720b51eeca96 36 fields · synced Jul 15, 2026
- EUDAMED 6d084792-4ced-4005-9808-80aa39385fc6 61 fields · synced Jul 15, 2026