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Operace

FDA UDI

Class I (US FDA UDI)

by Pb Swiss Tools Ag

Identity

Trade Name
OPERACE FDA UDI
Generic Name
Screw extractor, single-use FDA UDI
Device Name
Sterile single use insert for the removal of damaged screws FDA UDI
Model / Reference
80170 FDA UDI
Description
Sterile single use insert for the removal of damaged screws FDA UDI

Identifiers

Catalog Number
80170 FDA UDI
Primary DI / UDI-DI
07610733851706 FDA UDI
FDA Product Code
HWB FDA UDI
GMDN Term
Screw extractor, single-use 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

Yes

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Screw extractor, single-use

Operace by Pb Swiss Tools Ag — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Screw extractor, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Pb Swiss Tools Ag

Sources (1)

  • FDA UDI 962ae818-9fa6-45e8-8982-12d97b903634 35 fields · synced May 30, 2026