Identity
- Trade Name
- AMSCO FDA UDI
- Generic Name
- Medical device light source controller FDA UDI
- Device Name
- The Single Wall Controller is used with AMSCO LD202 Lighting System. FDA UDI
- Model / Reference
- LD202 FDA UDI
- Description
- The Single Wall Controller is used with AMSCO LD202 Lighting System. FDA UDI
Identifiers
- Catalog Number
- P141211178 FDA UDI
- Primary DI / UDI-DI
- 00724995161293 FDA UDI
- FDA Product Code
- KZF FDA UDI
- GMDN Term
- Medical device light source controller FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 880.6320 FDA UDI
- Commercial Distribution
- Not 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
Yes
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
Yes
FDA UDI
Amsco by Steris Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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 I | Pending data |
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Manufacturer
- Manufacturer
- Steris Corporation
Sources (1)
- FDA UDI ff2f3c6e-325a-4db0-9eab-746008e906f5 36 fields · synced Jun 8, 2026