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Estrogen Receptor RMab Control Slides

FDA UDI

Class I (US FDA UDI)

by Bio Sb, Inc.

Identity

Trade Name
Estrogen Receptor RMab Control Slides FDA UDI
Generic Name
Estrogen (oestrogen)/progesterone receptor IVD, control FDA UDI
Device Name
Estrogen Receptor RMab, Control FDA UDI
Model / Reference
Conrol Slides, 5 FDA UDI
Description
Estrogen Receptor RMab, Control FDA UDI

Identifiers

Catalog Number
BSB 2495 FDA UDI
Primary DI / UDI-DI
B502BSB24950 FDA UDI
FDA Product Code
LJG FDA UDI
GMDN Term
Estrogen (oestrogen)/progesterone receptor IVD, control FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
866.2660 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

No

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

No

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Safe FDA UDI

Category: Estrogen (oestrogen)/progesterone receptor IVD, control

Estrogen Receptor RMab Control Slides by Bio Sb, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Estrogen (oestrogen)/progesterone receptor IVD, control.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Bio Sb, Inc.

Sources (1)

  • FDA UDI d515c74f-fb49-4c6f-9ee5-7abea8ccb6a7 34 fields · synced May 30, 2026