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Breeze Centesis Drainage Catheterbreeze Centesis Drainage Catheter
FDA UDIClass I (US FDA UDI)
Identity
- Trade Name
- BREEZE CENTESIS DRAINAGE CATHETERBREEZE CENTESIS DRAINAGE CATHETER FDA UDI
- Generic Name
- Abdominal paracentesis needle, single-use FDA UDI
- Device Name
- 5F X 7CM BREEZE STRAIGHT5F X 7CM LUER LOCK CENTESISLUER LOCK CENT DRAINAGE CATHETERDRAINAGE CATHET FDA UDI
- Model / Reference
- CESLL5070 FDA UDI
- Description
- 5F X 7CM BREEZE STRAIGHT5F X 7CM LUER LOCK CENTESISLUER LOCK CENT DRAINAGE CATHETERDRAINAGE CATHET FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00884908131062 FDA UDI
- FDA Product Code
- GBX FDA UDI
- GMDN Term
- Abdominal paracentesis needle, single-use FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4200 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
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
Yes
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
Breeze Centesis Drainage Catheterbreeze Centesis Drainage Catheter by Medical Components Inc — Class I — FDA UDI — listed in FDA GUDID
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
- Medical Components Inc
Sources (1)
- FDA UDI d7a9801f-d781-4181-a575-2509d3571272 35 fields · synced Jun 1, 2026