← Back to catalogue

BMT Breast Shield

FDA UDI

Class I (US FDA UDI)

by Concure Oncology, Inc.

Identity

Trade Name
BMT Breast Shield FDA UDI
Generic Name
Patient radiation shielding pad/drape, reusable FDA UDI
Model / Reference
AC-B3110 FDA UDI

Identifiers

Primary DI / UDI-DI
00860003072776 FDA UDI
FDA Product Code
KPY FDA UDI
GMDN Term
Patient radiation shielding pad/drape, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
892.6500 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

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Patient radiation shielding pad/drape, reusable

BMT Breast Shield by Concure Oncology, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Patient radiation shielding pad/drape, reusable.

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 ac12753b-06b5-4ba5-861f-b9f8bc1e0c4a 32 fields · synced May 30, 2026