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Pure Buff

FDA UDI

Class I (US FDA UDI)

by Jordco, Inc.

Identity

Trade Name
Pure Buff FDA UDI
Generic Name
Dental laboratory mandrel FDA UDI
Device Name
Pure Buff Mandrels FDA UDI
Model / Reference
PBM-S FDA UDI
Description
Pure Buff Mandrels FDA UDI

Identifiers

Catalog Number
PBM-S FDA UDI
Primary DI / UDI-DI
00859611006204 FDA UDI
FDA Product Code
EHJ FDA UDI
GMDN Term
Dental laboratory mandrel FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.6010 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

Yes

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

Category: Dental laboratory mandrel

Pure Buff by Jordco, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental laboratory mandrel.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Jordco, Inc.

Sources (1)

  • FDA UDI 5daac5b3-48fe-4e9a-b386-cf59c9076020 34 fields · synced May 29, 2026