Identity
- Trade Name
- Collimator AL02 II eL FDA UDI
- Generic Name
- Manual-aperture-control diagnostic x-ray system collimator, motorized FDA UDI
- Model / Reference
- 10092614 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 04056869011578 FDA UDI
- FDA Product Code
- KPW FDA UDI
- GMDN Term
- Manual-aperture-control diagnostic x-ray system collimator, motorized FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 892.1610 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
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
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Manual-aperture-control diagnostic x-ray system collimator, motorized
Collimator AL02 II eL by Siemens Healthcare — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Siemens Healthcare
Sources (1)
- FDA UDI 8b02821a-9df7-4e77-af6e-c11701c2b959 34 fields · synced May 30, 2026