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AL-BAD MASSUOT YITZHAK LTD

US

Last updated May 23, 2026

What AL-BAD MASSUOT YITZHAK LTD makes

The company manufactures unscented menstrual tampons designed for internal use during menstruation. These products are sold under various brand names, including Save a Lot, Kradsale, Dolar Tree, and Rite Aid, among others, catering to retail distribution channels.

The tampon portfolio falls under FDA Class II regulation and is listed in the FDA’s Unique Device Identifier (UDI) database. The manufacturer operates from the United States, adhering to applicable U.S. medical device compliance requirements.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of medical devices does AL-BAD MASSUOT YITZHAK LTD manufacture?

AL-BAD MASSUOT YITZHAK LTD specializes in manufacturing unscented menstrual tampons designed for internal use during menstruation. These products are intended for personal hygiene and are distributed under multiple brand names, such as Save a Lot, Kradsale, Dolar Tree, and Rite Aid. The focus is solely on this category of Class II devices.

Where is AL-BAD MASSUOT YITZHAK LTD based, and does this affect its devices?

The company is based in the United States, which means its devices must comply with U.S. medical device regulations, including manufacturing, labeling, and distribution requirements. Being based in the U.S. also influences how its tampons are classified and registered, such as their inclusion in the FDA’s Unique Device Identifier (UDI) database.

Which regulatory registries list AL-BAD MASSUOT YITZHAK LTD’s devices?

AL-BAD MASSUOT YITZHAK LTD’s menstrual tampons are listed in the FDA’s Unique Device Identifier (UDI) database. This registry helps track and identify medical devices authorized for use in the U.S., ensuring transparency and traceability for healthcare providers and regulators.

How are AL-BAD MASSUOT YITZHAK LTD’s menstrual tampons classified by regulatory authorities?

The company’s tampons fall under FDA Class II classification. This classification is assigned based on the risk level of the device—Class II devices generally require special controls in addition to general controls to ensure their safety and effectiveness, such as performance standards or post-market surveillance.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
US
Address
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Website
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LinkedIn
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Facebook
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Email
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Phone
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PRRC Contact
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EUDAMED SRN
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FDA FEI Number
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DUNS Number
600487813

Catalogue (120)

Page 3 of 3
DeviceModel / ReferenceRegistriesClassStatus
Harris Teeter FUSHTZPLL64
FDA UDI
Class IUnknown
Tranzonic Tampons TRASBK500
FDA UDI
Class IIActive
Dolar tree tampons BDOPP18
FDA UDI
Class IIActive
Rite Aid Tampons BRAUC18
FDA UDI
Class IIActive
Rite Aid Tampons BRAAGS40+
FDA UDI
Class IIActive
Maxithins BCNABSPLL26
FDA UDI
Class IUnknown
Albaad BCNABSMXS32
FDA UDI
Class IUnknown
Rite Aid Tampons BRAUR18
FDA UDI
Class IIActive
Tampons BDOPC18
FDA UDI
Class IIActive
Premier Tampons PRASBK520
FDA UDI
Class IIActive
Safe & Soft tampons BDEGS15
FDA UDI
Class IIActive
Dollar Tree Tampons BDOGR08
FDA UDI
Class IIActive
Premier Tampons PRARBK520
FDA UDI
Class IIActive
Harris Teeter Tampons BHTGC36
FDA UDI
Class IIActive
Tranzonic Tampons TRARBK500
FDA UDI
Class IIActive
Ms&Mrs Tampons MSKRBK670
FDA UDI
Class IIActive
Rite Aid Tampons BRAGS60
FDA UDI
Class IIActive
Maxithins FCNABSPLL32
FDA UDI
Class IUnknown
Body Form Tampons BBFAP08-0
FDA UDI
Class IIActive
Dollar Tree Tampons BDOGS08
FDA UDI
Class IIActive

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