Identity
- Trade Name
- Atellica CH LIDO FDA UDI
- Generic Name
- Lidocaine therapeutic drug monitoring IVD, kit, nephelometry/turbidimetry FDA UDI
- Device Name
- Lidocaine (LIDO) Atellica CH - RGT 200T FDA UDI
- Model / Reference
- 11097539 FDA UDI
- Description
- Lidocaine (LIDO) Atellica CH - RGT 200T FDA UDI
Identifiers
- Catalog Number
- 11097539 FDA UDI
- Primary DI / UDI-DI
- 00630414220680 FDA UDI
- 510(k) Number
- K033809 FDA UDI
- FDA Product Code
- KLR FDA UDI
- GMDN Term
- Lidocaine therapeutic drug monitoring IVD, kit, nephelometry/turbidimetry FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 862.3555 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
No
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
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Lidocaine therapeutic drug monitoring IVD, kit, nephelometry/turbidimetry
Atellica CH LIDO by Siemens Healthcare Diagnostics — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Lidocaine therapeutic drug monitoring IVD, kit, nephelometry/turbidimetry.
Cleared under the same submission
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 Diagnostics
Sources (1)
- FDA UDI 309fd27a-9974-4a30-b1f8-5bf5c8033478 37 fields · synced May 30, 2026