← Back to catalogue

Pointe Scientific, Inc.

FDA UDI

by Pointe Scientific, Inc.

Identity

Trade Name
Pointe Scientific, Inc. FDA UDI
Generic Name
Albumin IVD, kit, spectrophotometry FDA UDI
Device Name
Albumin, for the quantitative determination of Albumin in serum on the Hitachi 917 analyzer. Size: 12 x 66mL FDA UDI
Model / Reference
HA902-792 FDA UDI
Description
Albumin, for the quantitative determination of Albumin in serum on the Hitachi 917 analyzer. Size: 12 x 66mL FDA UDI

Identifiers

Catalog Number
HA902-792 FDA UDI
Primary DI / UDI-DI
00811727012869 FDA UDI
510(k) Number
K822471 FDA UDI
GMDN Term
Albumin IVD, kit, spectrophotometry FDA UDI

Classification

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: Albumin IVD, kit, spectrophotometry

Pointe Scientific, Inc. by Pointe Scientific, Inc. — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Albumin IVD, kit, spectrophotometry.

Cleared under the same submission

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

Sources (1)

  • FDA UDI a0bb05ad-4eca-4081-ad71-afa6ff8b6af1 37 fields · synced Jun 8, 2026