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Meijer Tampon

FDA UDI

Class II (US FDA UDI)

by Meijer, Inc.

Identity

Trade Name
Meijer Tampon FDA UDI
Generic Name
Menstrual tampon, unscented FDA UDI
Device Name
Multipack of 36 tampons, 8 Regular, 20 Super and 8 Super plus absorbency FDA UDI
Model / Reference
BMEGC36 FDA UDI
Description
Multipack of 36 tampons, 8 Regular, 20 Super and 8 Super plus absorbency FDA UDI

Identifiers

Primary DI / UDI-DI
00708820693388 FDA UDI
FDA Product Code
HEB FDA UDI
GMDN Term
Menstrual tampon, unscented FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
884.5470 FDA UDI
Commercial Distribution
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

Yes

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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Menstrual tampon, unscented

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

Similar devices

Also classified as Menstrual tampon, unscented.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Meijer, Inc.

Sources (1)

  • FDA UDI 676011a6-6d89-4f83-a8a5-939ee2cec75e 34 fields · synced May 30, 2026