OTOCELL® Instrument Wipe

FDA UDI

Class I (US FDA UDI)

by Boston Medical Products, Inc.

Identity

Trade Name: OTOCELL® Instrument Wipe FDA UDI
Generic Name: Dry medical towel/wipe, single-use FDA UDI
Device Name: Size: 0.1 x 8.25 x 8.25 cm FDA UDI
Model / Reference: WP-881 FDA UDI
Description: Size: 0.1 x 8.25 x 8.25 cm FDA UDI

Identifiers

Catalog Number: WP-881 FDA UDI
Primary DI / UDI-DI: EBESWP8810 FDA UDI
FDA Product Code: NAB FDA UDI
GMDN Term: Dry medical towel/wipe, single-use FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 878.4014 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

MRI Safety

MR Safe FDA UDI

Dimensions & Sizes

Size: Width — 0.1 Centimeter FDA UDI
Height — 8.25 Centimeter FDA UDI
Length — 8.25 Centimeter FDA UDI

Category: Dry medical towel/wipe, single-use

OTOCELL® Instrument Wipe by Boston Medical Products, Inc. — 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: Boston Medical Products, Inc.

Sources (1)

FDA UDI cda48b74-aaf6-4411-ab97-aa9cebc6eaf9 37 fields · synced Jun 9, 2026