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Fresenius

FDA UDI

Class II (US FDA UDI)

by Fresenius Medical Care Holdings, Inc.

Identity

Trade Name
Fresenius FDA UDI
Generic Name
Haemodialysis blood tubing set, single-use FDA UDI
Device Name
Priming Set FDA UDI
Model / Reference
04-9006-5 FDA UDI
Description
Priming Set FDA UDI

Identifiers

Catalog Number
04-9006-5 FDA UDI
Primary DI / UDI-DI
00840861100514 FDA UDI
510(k) Number
K010268 FDA UDI
FDA Product Code
KOC 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

No

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

Fresenius by Fresenius Medical Care Holdings, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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 809619ed-b2f1-4eee-a016-d27d0ac9e280 36 fields · synced May 30, 2026