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Signature Care

FDA UDI

Class II (US FDA UDI)

by Better Living Brands Llc

Identity

Trade Name
Signature Care FDA UDI
Generic Name
Total human chorionic gonadotropin IVD, kit, rapid ICT, clinical FDA UDI
Device Name
CB8 Digital Pregnancy Stick Signature Care DPS Digital Early FDA UDI
Model / Reference
Digital Pregnancy Test FDA UDI
Description
CB8 Digital Pregnancy Stick Signature Care DPS Digital Early FDA UDI

Identifiers

Primary DI / UDI-DI
00021130790050 FDA UDI
510(k) Number
K060128 FDA UDI
FDA Product Code
LCX FDA UDI
GMDN Term
Total human chorionic gonadotropin IVD, kit, rapid ICT, clinical FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.1155 FDA UDI
Commercial Distribution
Not 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

Yes

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Signature Care by Better Living Brands Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 61ef4bc2-58c8-4039-b4ec-baf725122b93 37 fields · synced May 30, 2026