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TQE Plus Endotoxin 30" Filter Flat 222 Head

FDA UDI

Class II (US FDA UDI)

by Nephros, Inc.

Identity

Trade Name
TQE Plus Endotoxin 30" Filter Flat 222 Head FDA UDI
Generic Name
Peritoneal dialysis system dialysate filter FDA UDI
Device Name
The TQE PlusEndotoxinFilter(Flat)is a hollow fiber ultrafilter that retains bacteria and endotoxin from fluid. FDA UDI
Model / Reference
TQE0.005-30P3E FDA UDI
Description
The TQE PlusEndotoxinFilter(Flat)is a hollow fiber ultrafilter that retains bacteria and endotoxin from fluid. FDA UDI

Identifiers

Primary DI / UDI-DI
00868277000433 FDA UDI
510(k) Number
K161304 FDA UDI
FDA Product Code
FIP FDA UDI
GMDN Term
Peritoneal dialysis system dialysate filter FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.5665 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
Sterilization Method
Liquid Chemical FDA UDI

TQE Plus Endotoxin 30" Filter Flat 222 Head by Nephros, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Nephros, Inc.

Sources (1)

  • FDA UDI 93b39d0f-a476-4c3a-8ed4-792be28be137 35 fields · synced Jun 6, 2026