Dr. Talbot's

FDA UDI

Class I (US FDA UDI)

by Talbot's Pharmaceuticals Family Products Llc

Identity

Trade Name: Dr. Talbot's FDA UDI
Generic Name: Natural conception assistance kit FDA UDI
Model / Reference: 1101 FDA UDI

Identifiers

Primary DI / UDI-DI: 00370797011016 FDA UDI
FDA Product Code: CEP FDA UDI
LCX FDA UDI
GMDN Term: Natural conception assistance kit FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 862.1485 FDA UDI
862.1155 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Category: Total human chorionic gonadotropin IVD, kit, rapid ICT, clinical Natural conception assistance kit

Dr. Talbot's by Talbot's Pharmaceuticals Family Products Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Talbot's Pharmaceuticals Family Products Llc

Sources (1)

FDA UDI f8cbef21-5785-48f5-bab8-8e35ab8622f8 32 fields · synced May 30, 2026