← Back to catalogue

Lola

FDA UDI

Class II (US FDA UDI)

by Alyk, Inc.

Identity

Trade Name
LOLA FDA UDI
Generic Name
Menstrual cup/disc, non-latex, reusable FDA UDI
Model / Reference
Menstrual Cup Size 2 FDA UDI

Identifiers

Primary DI / UDI-DI
00850017666412 FDA UDI
FDA Product Code
HHE FDA UDI
GMDN Term
Menstrual cup/disc, non-latex, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
884.5400 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

Category: Menstrual cup/disc, non-latex, reusable

Lola by Alyk, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Menstrual cup/disc, non-latex, 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

Manufacturer
Alyk, Inc.

Sources (1)

  • FDA UDI 8970c92d-a463-4962-8e11-994662ff9731 32 fields · synced May 30, 2026