← Back to catalogue

Rexall 7-Day Contour Pill Reminder

FDA UDI

Class I (US FDA UDI)

by Shanghai Care US Medical Product Co., Ltd.

Identity

Trade Name
Rexall 7-Day Contour Pill Reminder FDA UDI
Generic Name
Pill crusher/splitter FDA UDI
Model / Reference
A0363 FDA UDI

Identifiers

Primary DI / UDI-DI
06970285515565 FDA UDI
FDA Product Code
NXB FDA UDI
GMDN Term
Pill crusher/splitter FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.5050 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

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

Yes

FDA UDI

Category: Pill crusher/splitter

Rexall 7-Day Contour Pill Reminder by Shanghai Care US Medical Product Co., Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Pill crusher/splitter.

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 a5e0c492-1a23-4d95-aea7-c63e11d23fc1 32 fields · synced Jun 8, 2026