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Quinelato

FDA UDI

Class I (US FDA UDI)

by Schobell Industrial Ltda

Identity

Trade Name
Quinelato FDA UDI
Generic Name
ENT wire-cutting scissors FDA UDI
Device Name
Bee Bee bone scissors 18cm FDA UDI
Model / Reference
QT.996.18 FDA UDI
Description
Bee Bee bone scissors 18cm FDA UDI

Identifiers

Catalog Number
QT.996.18 FDA UDI
Primary DI / UDI-DI
07898506845378 FDA UDI
FDA Product Code
NNU FDA UDI
GMDN Term
ENT wire-cutting scissors FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
874.3540 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: ENT wire-cutting scissors

Quinelato by Schobell Industrial Ltda — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as ENT wire-cutting scissors.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI f47ec5db-a3e6-490a-a780-7575f44d8cd8 34 fields · synced Jun 8, 2026