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BOSS Instruments

FDA UDI

Class I (US FDA UDI)

by Boss Instruments, Ltd.

Identity

Trade Name
BOSS Instruments FDA UDI
Generic Name
Nasal speculum, reusable FDA UDI
Device Name
Cottle Spec, 90mm blds, 10mm to 8mm taper FDA UDI
Model / Reference
93-1737 FDA UDI
Description
Cottle Spec, 90mm blds, 10mm to 8mm taper FDA UDI

Identifiers

Catalog Number
93-1737 FDA UDI
Primary DI / UDI-DI
00888515241923 FDA UDI
FDA Product Code
EPY FDA UDI
GMDN Term
Nasal speculum, reusable 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

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Nasal speculum, reusable

BOSS Instruments by Boss Instruments, Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Nasal speculum, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI ce3ad13f-5ae4-4e2d-bbf2-6c9364b48c47 35 fields · synced Jun 9, 2026