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PureSet™

FDA UDI

Class II (US FDA UDI)

by Nobel Biocare AG

Identity

Trade Name
PureSet™ FDA UDI
Generic Name
Instrument tray, reusable FDA UDI
Device Name
NobelParallel™ CC Guided PureSet Tray Plate FDA UDI
Model / Reference
PUR0701 FDA UDI
Description
NobelParallel™ CC Guided PureSet Tray Plate FDA UDI

Identifiers

Catalog Number
PUR0701 FDA UDI
Primary DI / UDI-DI
07332747169072 FDA UDI
510(k) Number
K181075 FDA UDI
FDA Product Code
KCT FDA UDI
GMDN Term
Instrument tray, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.6850 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

No

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size
Height — 2.000 Millimeter FDA UDI
Width — 165.000 Millimeter FDA UDI
Length — 260.000 Millimeter FDA UDI

Category: Instrument tray, reusable

PureSet™ by Nobel Biocare AG — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Instrument tray, reusable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Nobel Biocare AG

Sources (1)

  • FDA UDI bbbe8de0-d409-498c-abd8-6a276a9046b9 37 fields · synced May 30, 2026