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shaft obturator
FDA UDIEUDAMEDClass I (US FDA UDI)
Ref ASBO02110
by Joimax, Inc.
Identity
- Trade Name
- Shaft-Obturator blunt for Arthroscope Shaft EUDAMEDshaft obturator FDA UDI
- Generic Name
- Rigid endoscope obturator FDA UDI
- Device Name
- Shaft obturator for endoscope shaft EUDAMEDShaft-Obturator blunt for Arthroscope Shaft FDA UDI
- Model / Reference
- ASBO02110 EUDAMEDFDA UDI
- Description
- Shaft-Obturator blunt for Arthroscope Shaft FDA UDI
Identifiers
- Catalog Number
- ASBO02110 FDA UDI
- Primary DI / UDI-DI
- 04250337100058 EUDAMEDFDA UDI
- Basic UDI-DI
- 42503371ENSCOBTGK EUDAMED
- Direct Marketing DI
- 04250337100058 EUDAMED
- FDA Product Code
- NBH FDA UDI
- EMDN Code
- Z12021199 ORTHOPAEDIC ENDOSCOPY INSTRUMENTS - OTHER EUDAMED
- GMDN Term
- Rigid endoscope obturator FDA UDI
Classification
- Device Class
- Class I EUDAMEDFDA 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: Rigid endoscope obturator
shaft obturator by Joimax, Inc. — Class I — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS
Similar devices
Also classified as Rigid endoscope obturator.
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- USA Elite — Gyrus Acmi, Inc. · Class II
- Trabecular Metal® — Zimmer, Inc. · Class I
- SHARK — Richard Wolf GmbH · Class II
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
- Joimax, Inc.
Sources (2)
- FDA UDI bdc7e971-8cf9-4ce6-b97d-0a7c87145d3e 36 fields · synced Jul 22, 2026
- EUDAMED 935aaacb-f810-4ea4-8520-ab3f9717348b 61 fields · synced Jul 22, 2026