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Pointe Glucose Hexokinase for BS480

FDA UDI

Class II (US FDA UDI)

by Pointe Scientific, Inc.

Identity

Trade Name
Pointe Glucose Hexokinase for BS480 FDA UDI
Generic Name
Glucose IVD, kit, spectrophotometry FDA UDI
Device Name
Pointe Glucose Hexokinase Reagent packaged for use on the BS480. 8x60 mL Kit. For the in vitro quantitative measurement of glucose in serum. FDA UDI
Model / Reference
14-G7517-480 FDA UDI
Description
Pointe Glucose Hexokinase Reagent packaged for use on the BS480. 8x60 mL Kit. For the in vitro quantitative measurement of glucose in serum. FDA UDI

Identifiers

Catalog Number
14-G7517-480 FDA UDI
Primary DI / UDI-DI
00811727015846 FDA UDI
510(k) Number
K961282 FDA UDI
FDA Product Code
CFR FDA UDI
GMDN Term
Glucose IVD, kit, spectrophotometry FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.1345 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: Glucose IVD, kit, spectrophotometry

Pointe Glucose Hexokinase for BS480 by Pointe Scientific, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Glucose 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 119c5dd0-a268-4535-bbf6-74551e91903c 37 fields · synced May 30, 2026