← Back to catalogue

Tablo Hemodialysis Concentrate

FDA UDI

Class II (US FDA UDI)

by Outset Medical, Inc.

Identity

Trade Name
Tablo Hemodialysis Concentrate FDA UDI
Generic Name
Haemodialysis concentrate FDA UDI
Device Name
Liquid acid concentrate, 45X, 2K, 2.5Ca, 1 U.S. gallon FDA UDI
Model / Reference
PN-0000832 FDA UDI
Description
Liquid acid concentrate, 45X, 2K, 2.5Ca, 1 U.S. gallon FDA UDI

Identifiers

Catalog Number
A-225 FDA UDI
Primary DI / UDI-DI
00850001011044 FDA UDI
FDA Product Code
FKQ FDA UDI
GMDN Term
Haemodialysis concentrate 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

No

FDA UDI

Single Use

No

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Haemodialysis concentrate

Tablo Hemodialysis Concentrate by Outset Medical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Haemodialysis concentrate.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 3ac382b0-8280-49fb-8701-d91359eaadc8 36 fields · synced May 30, 2026