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LIPASE Color

FDA UDI

Class I (US FDA UDI)

by Sekisui Diagnostics, LLC

Identity

Trade Name
LIPASE Color FDA UDI
Generic Name
Lipase IVD, kit, spectrophotometry FDA UDI
Model / Reference
905-B FDA UDI

Identifiers

Catalog Number
905-B FDA UDI
Primary DI / UDI-DI
00628063400782 FDA UDI
510(k) Number
K897150 FDA UDI
FDA Product Code
CHI FDA UDI
GMDN Term
Lipase IVD, kit, spectrophotometry FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.1465 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

Yes

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: Lipase IVD, kit, spectrophotometry

LIPASE Color by Sekisui Diagnostics, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Lipase IVD, kit, spectrophotometry.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI b3f60bc0-2fe1-4925-af46-a4b7204e9f49 34 fields · synced Jun 9, 2026