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Hgb Control, High

FDA UDI

Class I (US FDA UDI)

by Stanbio Laboratory, L.p.

Identity

Trade Name
Hgb Control, High FDA UDI
Generic Name
Total haemoglobin (totHb) IVD, control FDA UDI
Device Name
A single level reference control intended for use on HemoPoint® H2 Hemoglobin testing system. FDA UDI
Model / Reference
3060-101H FDA UDI
Description
A single level reference control intended for use on HemoPoint® H2 Hemoglobin testing system. FDA UDI

Identifiers

Catalog Number
3060-101H FDA UDI
Primary DI / UDI-DI
00657498002032 FDA UDI
FDA Product Code
JJY FDA UDI
GMDN Term
Total haemoglobin (totHb) IVD, control FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.1660 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Total haemoglobin (totHb) IVD, control

Hgb Control, High by Stanbio Laboratory, L.p. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Total haemoglobin (totHb) IVD, control.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 168d29b2-b404-4cb1-a28f-da464a4f4455 36 fields · synced Jun 6, 2026