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Lola

FDA UDI

Class I (US FDA UDI)

by Alyk, Inc.

Identity

Trade Name
LOLA FDA UDI
Generic Name
Menstrual underwear FDA UDI
Model / Reference
Washable Period Underwear Size Large FDA UDI

Identifiers

Primary DI / UDI-DI
00850017666863 FDA UDI
FDA Product Code
NUQ FDA UDI
GMDN Term
Menstrual underwear FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
884.5435 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

Yes

FDA UDI

Category: Menstrual underwear

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

Similar devices

Also classified as Menstrual underwear.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Alyk, Inc.

Sources (1)

  • FDA UDI 24e09e85-7cb6-462b-897b-bea0cc865e9c 32 fields · synced May 30, 2026