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Lipase

FDA UDI

Class I (US FDA UDI)

by Pointe Scientific, Inc.

Identity

Trade Name
Lipase FDA UDI
Generic Name
Lipase IVD, kit, spectrophotometry FDA UDI
Device Name
For the in vitro quantitative kinetic determination of Pancreatic Lipase in serum. FDA UDI
Model / Reference
12-L7503-40 FDA UDI
Description
For the in vitro quantitative kinetic determination of Pancreatic Lipase in serum. FDA UDI

Identifiers

Catalog Number
12-L7503-40 FDA UDI
Primary DI / UDI-DI
00811727013613 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 by Pointe Scientific, Inc. — 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 5ef35492-b901-4482-b103-2881edda563b 37 fields · synced Jun 8, 2026