Identity
- Trade Name
- Low Pressure Connector Tubing FDA UDI
- Generic Name
- Radiographic procedure tubing FDA UDI
- Device Name
- "Envision, Vistron, MCT - Coiled 60"" Low Pressure Connector Tube (SET, PKG, LPDCT 160, RAD, MC,JA) (84194913)" FDA UDI
- Model / Reference
- LPDCT 160 FDA UDI
- Description
- "Envision, Vistron, MCT - Coiled 60"" Low Pressure Connector Tube (SET, PKG, LPDCT 160, RAD, MC,JA) (84194913)" FDA UDI
Identifiers
- Catalog Number
- LPDCT 160 FDA UDI
- Primary DI / UDI-DI
- 00616258007281 FDA UDI
- FDA Product Code
- DOY FDA UDI
- GMDN Term
- Radiographic procedure tubing FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 862.3320 FDA UDI
- Commercial Distribution
- 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
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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Radiographic procedure tubing
Low Pressure Connector Tubing by Bayer Medical Care Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Radiographic procedure tubing.
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- Solution Transfer Device — Bracco Diagnostics Inc. · Class II
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
- Bayer Medical Care Inc.
Sources (1)
- FDA UDI 63ce1377-1fc0-494c-b264-1cc09c38b8ac 35 fields · synced Jun 9, 2026