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BV Medical

FDA UDI

Class I (US FDA UDI)

by Medical, Inc.

Identity

Trade Name
BV Medical FDA UDI
Generic Name
Ear speculum, single-use FDA UDI
Device Name
Otoscope Specula Variety Pack: 25 each of 2.5, 3.0, 4.0, 5.0 (Black, Latex Free) FDA UDI
Model / Reference
61-600-010 FDA UDI
Description
Otoscope Specula Variety Pack: 25 each of 2.5, 3.0, 4.0, 5.0 (Black, Latex Free) FDA UDI

Identifiers

Primary DI / UDI-DI
00845821026484 FDA UDI
FDA Product Code
FXG FDA UDI
GMDN Term
Ear speculum, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.1800 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

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Ear speculum, single-use

BV Medical by Medical, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ear speculum, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medical, Inc.

Sources (1)

  • FDA UDI e9ee18f5-94f7-4ee8-aed7-5aba1c025eb7 34 fields · synced May 30, 2026