Identity
- Trade Name
- simex FDA UDI
- Generic Name
- Suction system catheter, general-purpose FDA UDI
- Device Name
- Suction tube, sterile, CH21, 180cm with clamp, funnel and luer connector FDA UDI
- Model / Reference
- suction tube CH21 FDA UDI
- Description
- Suction tube, sterile, CH21, 180cm with clamp, funnel and luer connector FDA UDI
Identifiers
- Catalog Number
- 112203 FDA UDI
- Primary DI / UDI-DI
- 04052262413513 FDA UDI
- FDA Product Code
- GAZ FDA UDI
- GMDN Term
- Suction system catheter, general-purpose FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.6740 FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
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
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
simex by Simex Medizintechnik GmbH — Class II — 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 II | Pending data |
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Manufacturer
- Manufacturer
- Simex Medizintechnik GmbH
Sources (1)
- FDA UDI 9c35ab7e-731e-4424-857e-b8c009020b00 36 fields · synced May 30, 2026