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Slimline™ Blood Tubing Set With Transducer Protectors And Priming Set

FDA UDI

Class II (US FDA UDI)

by Nipro Medical Corporation

Identity

Trade Name
SLIMLINE™ BLOOD TUBING SET WITH TRANSDUCER PROTECTORS AND PRIMING SET FDA UDI
Generic Name
Haemodialysis blood tubing set, single-use FDA UDI
Device Name
Slimline Blood Tubing for Fresenius 2008H, K, K2, T FDA UDI
Model / Reference
BL+A226Y/V813-NIJ FDA UDI
Description
Slimline Blood Tubing for Fresenius 2008H, K, K2, T FDA UDI

Identifiers

Primary DI / UDI-DI
00383790011877 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
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

Category: Haemodialysis blood tubing set, single-use

Slimline™ Blood Tubing Set With Transducer Protectors And Priming Set by Nipro Medical Corporation — Class II — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Haemodialysis blood tubing set, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI e5215af7-53e1-491c-861e-1b8132324498 33 fields · synced Jun 8, 2026