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Quinelato

FDA UDI

Class I (US FDA UDI)

by Schobell Industrial Ltda

Identity

Trade Name
Quinelato FDA UDI
Generic Name
Bone holding forceps FDA UDI
Device Name
Spanish Bone Reduction Forceps 16cm FDA UDI
Model / Reference
QO.397.16 FDA UDI
Description
Spanish Bone Reduction Forceps 16cm FDA UDI

Identifiers

Catalog Number
QO.397.16 FDA UDI
Primary DI / UDI-DI
07898506848614 FDA UDI
FDA Product Code
LXH FDA UDI
GMDN Term
Bone holding forceps FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 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: Bone holding forceps

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

Similar devices

Also classified as Bone holding forceps.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Schobell Industrial Ltda

Sources (1)

  • FDA UDI 1b5efd2f-9b7d-41a2-959b-f6037e4aa70f 34 fields · synced May 30, 2026