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ACK Lysing Buffer

FDA UDI

Class I (US FDA UDI)

by Lonza Walkersville, Inc.

Identity

Trade Name
ACK Lysing Buffer FDA UDI
Generic Name
Ex vivo cell culture medium FDA UDI
Model / Reference
08-974H FDA UDI

Identifiers

Catalog Number
08-974H FDA UDI
Primary DI / UDI-DI
00840075403036 FDA UDI
FDA Product Code
PPM FDA UDI
GMDN Term
Ex vivo cell culture medium FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
864.4010 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

No

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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Ex vivo cell culture medium

ACK Lysing Buffer by Lonza Walkersville, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ex vivo cell culture medium.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI d39ca6f5-c188-4173-a9cf-0bd07d2ed841 33 fields · synced Jun 1, 2026