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Custom Healthcare Systems Inc.

FDA UDI

Class II (US FDA UDI)

by Manus Medical, LLC

Identity

Trade Name
Custom Healthcare Systems Inc. FDA UDI
Generic Name
Mammographic stereotactic biopsy system FDA UDI
Model / Reference
B446MM-B FDA UDI

Identifiers

Primary DI / UDI-DI
00811870031137 FDA UDI
FDA Product Code
LRO FDA UDI
GMDN Term
Mammographic stereotactic biopsy system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4370 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

Yes

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Ethylene Oxide FDA UDI

Category: Mammographic stereotactic biopsy system

Custom Healthcare Systems Inc. by Manus Medical, LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Mammographic stereotactic biopsy system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Manus Medical, LLC

Sources (1)

  • FDA UDI ae5952d2-2875-495f-bbab-88381945bd29 32 fields · synced Jun 1, 2026