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Leibinger ZD frame Mechanical Set KIT
EUDAMEDFDA UDIClass I (EU MDR)
Ref 700-020847-00Model 700-020834-00
Identity
- Trade Name
- Leibinger ZD frame Mechanical Set KIT EUDAMEDFDA UDI
- Generic Name
- Depth electrode FDA UDI
- Device Name
- CRW Non-XY frame Mechanical Set KIT EUDAMED
- Model / Reference
- 700-020834-00 EUDAMED700-020847-00 EUDAMED4 FDA UDI
Identifiers
- Catalog Number
- 700-020847-00 FDA UDI
- Primary DI / UDI-DI
- 27290114061128 EUDAMEDFDA UDI
- Basic UDI-DI
- 729011406123MECHB EUDAMED
- 510(k) Number
- K051830 FDA UDI
- FDA Product Code
- GZL FDA UDI
- EMDN Code
- N010199 NEUROPHYSIOLOGY DEVICES - OTHER EUDAMED
- GMDN Term
- Depth electrode FDA UDI
Classification
- Device Class
- Class I EUDAMEDClass II FDA UDI
- Regulation Number
- 882.1330 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
No
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Dry Heat Sterilization FDA UDI
MR Unsafe FDA UDI
Leibinger ZD frame Mechanical Set KIT by Alpha Omega Engineering Ltd — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/MDR
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 729011406123MECHB | Class I | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Alpha Omega Engineering Ltd
- EUDAMED SRN
- IL-MF-000025214
- Authorised Representative
- Alpha Omega GmbH DE-AR-000022420
Sources (2)
- EUDAMED 4622a9b4-5196-4681-90a0-dc5f8cc3fe0f 61 fields · synced Jun 6, 2026
- FDA UDI b0378044-4329-40bb-926b-e15c1ac84e2d 34 fields · synced May 30, 2026