← Back to catalogue

Plasmalink Transfer-Pack Container - 2000 mL

FDA UDI

Class II (US FDA UDI)

by Fresenius Kabi

Identity

Trade Name
Plasmalink Transfer-Pack Container - 2000 mL FDA UDI
Generic Name
Blood/tissue storage/culture container FDA UDI
Device Name
For processing and/or storage of blood and blood components. Sterile Fluid Path. FDA UDI
Model / Reference
6R2042 FDA UDI
Description
For processing and/or storage of blood and blood components. Sterile Fluid Path. FDA UDI

Identifiers

Catalog Number
6R2042 FDA UDI
Primary DI / UDI-DI
00810020440669 FDA UDI
FDA Product Code
KSR FDA UDI
GMDN Term
Blood/tissue storage/culture container FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
864.9100 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
Sterilization Method
Radiation Sterilization FDA UDI

Category: Blood/tissue storage/culture container

Plasmalink Transfer-Pack Container - 2000 mL by Fresenius Kabi — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Blood/tissue storage/culture container.

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

Manufacturer
Fresenius Kabi

Sources (1)

  • FDA UDI 784baccc-dde4-48db-9bb5-ac653d2eeff4 36 fields · synced May 30, 2026