Cirq Robotic Alignment Module
EUDAMEDFDA UDIFDA 510(k)Class I (EU MDR)
by Brainlab SE
Identity
- Trade Name
- Cirq Robotic Alignment Module EUDAMEDFDA UDI
- Generic Name
- Surgical instrument assist arm system, power-adjusted FDA UDI
- Device Name
- Cirq Robotic Alignment Module EUDAMED
- Model / Reference
- 56100 EUDAMEDFDA UDI
Identifiers
- Catalog Number
- 56100 FDA UDI
- Primary DI / UDI-DI
- 04056481141646 EUDAMEDFDA UDI
- Basic UDI-DI
- 4056481MotorUnitU2 EUDAMED
- FDA Product Code
- HAW FDA UDIOLO FDA UDI
- EMDN Code
- Z12011480 SURGICAL NAVIGATION INSTRUMENTS - HARDWARE ACCESSORIES EUDAMED
- GMDN Term
- Surgical instrument assist arm system, power-adjusted FDA UDI
Classification
- Device Class
- Class I EUDAMEDClass II FDA UDI
- Regulation Number
- 882.4560 FDA UDI
- Market of Registration
- Germany EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
Single Use
No
Implantable
No
Reusable
No
Contains Latex
No
Reprocessed
No
CMR Substance
No
Human-derived
No
Human Tissues
No
Animal Tissues
No
Endocrine Disruptor
No
Administering Medicine
No
Measuring Function
No
Incorporates Medicinal Product
No
Prescription Use
Yes
Over-the-Counter
No
Convenience Kit
No
Combination Product
No
HCT/P
No
Premarket Exempt
No
Lot / Batch Number
No
Serial Number
Yes
Expiration Date
No
Manufacturing Date
No
Category: Neurological stereotactic surgery system
Cirq Robotic Alignment Module by Brainlab SE — Class I — FDA_510K, MDR — listed in EUDAMED, FDA GUDID, FDA 510(k) — regulatory data on deviCERTS
Similar devices
Also classified as Neurological stereotactic surgery system.
- PEEK INSTRUMENT ADAPTOR Ø2.15MM — MEDTECH LLC · Class II
- Mini-Bolt VUE Accessory Kit — MONTERIS MEDICAL CORP · Class I
- StealthAiR™ Spine — MEDTRONIC NAVIGATION, INC. · Class II
- StealthStation — MEDTRONIC NAVIGATION, INC. · Class II
- OsteoMed™ Manual Driver Handle — FHC, INC. · Class II
- PMT CORPORATION - STEREOTACTIC — Pmt Corp. · Class II
- Leksell Stereotactic System — Elekta Instrument AB · Class II
- Leksell Stereotactic System — Elekta Instrument AB · Class II
Authorization Coverage (2 countries)
Regulatory Authorizations
FDA_510K
CE/MDR
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA 510(k) | United States | FDA_510K | K202320 | Class I | Active |
| EUDAMED | European Union | CE/MDR | 4056481MotorUnitU2 | Class I | Active |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Brainlab SE
- EUDAMED SRN
- DE-MF-000006183
Sources (3)
- EUDAMED c1e00841-7630-4e38-8b34-f037376fc06a 61 fields · synced Jul 9, 2026
- FDA UDI 73ec2839-1bc0-44a0-8e3f-2f3aaef83c4f 34 fields · synced May 30, 2026
- FDA 510(k) K202320 1 fields · synced May 18, 2026