← Back to catalogue
Streamline Airless System Set with Locksite Needleless Access Sites
FDA UDIClass II (US FDA UDI)
Identity
- Trade Name
- Streamline Airless System Set with Locksite Needleless Access Sites FDA UDI
- Generic Name
- Haemodialysis blood tubing set, single-use FDA UDI
- Model / Reference
- SL-2000M2095 FDA UDI
Identifiers
- Primary DI / UDI-DI
- M535SL2000M20950 FDA UDI
- FDA Product Code
- FJK FDA UDI
- GMDN Term
- Haemodialysis blood tubing set, single-use FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 876.5820 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
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
Streamline Airless System Set with Locksite Needleless Access Sites by Medisystems Corp. — Class II — 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 II | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Medisystems Corp.
Sources (1)
- FDA UDI f6b4f5d4-1519-4db4-bc02-894a21c74240 35 fields · synced May 30, 2026