← Back to catalogue

Malem

FDA UDI

Class I (US FDA UDI)

by Malem Medical Limited

Identity

Trade Name
Malem FDA UDI
Generic Name
Bladder-emptying vibratory stimulator FDA UDI
Device Name
Queen's Square Bladder Stimulator (PC9) FDA UDI
Model / Reference
PC9 FDA UDI
Description
Queen's Square Bladder Stimulator (PC9) FDA UDI

Identifiers

Primary DI / UDI-DI
05060049630199 FDA UDI
FDA Product Code
ISA FDA UDI
GMDN Term
Bladder-emptying vibratory stimulator FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.5660 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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Bladder-emptying vibratory stimulator

Malem by Malem Medical Limited — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bladder-emptying vibratory stimulator.

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 c1dc89db-cae3-4b8a-9d01-c8d229255f83 33 fields · synced Jun 7, 2026