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SAMI RRT Cassette

FDA UDI

Class II (US FDA UDI)

by Spectral Medical Inc

Identity

Trade Name
SAMI RRT Cassette FDA UDI
Generic Name
Haemodialysis blood tubing set, single-use FDA UDI
Device Name
The SAMI RRT Cassette is provided sterile, single use only, and has a non-toxic, non-pyrogenic fluid path. The package is sterile if the package is intact, undamaged, and protective caps are secure. The cassette tubing set is a single line set including venous and arterial blood paths and is provided as a single unit in a sterile pouch. FDA UDI
Model / Reference
SA-400-00 FDA UDI
Description
The SAMI RRT Cassette is provided sterile, single use only, and has a non-toxic, non-pyrogenic fluid path. The package is sterile if the package is intact, undamaged, and protective caps are secure. The cassette tubing set is a single line set including venous and arterial blood paths and is provided as a single unit in a sterile pouch. FDA UDI

Identifiers

Catalog Number
SA-400-00 FDA UDI
Primary DI / UDI-DI
B173SA400000 FDA UDI
FDA Product Code
KDI FDA UDI
GMDN Term
Haemodialysis blood tubing set, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.5860 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

SAMI RRT Cassette by Spectral Medical Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 61eb8200-e8b8-440a-a6bc-2f2d2beb8939 37 fields · synced Jun 8, 2026