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Streamline Airless System Set with Locksite Needleless Access Sites

FDA UDI

Class II (US FDA UDI)

by NxStage Medical, Inc.

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-2050M2055 FDA UDI

Identifiers

Primary DI / UDI-DI
M535SL2050M20550 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 NxStage Medical, Inc. — Class II — FDA UDI — listed in FDA GUDID

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
NxStage Medical, Inc.

Sources (1)

  • FDA UDI 4353d1a2-013d-4e60-ac9d-7a7daf7f658b 35 fields · synced Jun 9, 2026