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Pele Tim

FDA UDIEUDAMED

Class I (US FDA UDI)

by VOCO GmbH

Identity

Trade Name
Pele Tim FDA UDI
Generic Name
Dental material application tool, single-use FDA UDI
Device Name
Pele Tim - No. 4 500 x 6 x 8 mm FDA UDI
Model / Reference
2255 FDA UDI
Description
Pele Tim - No. 4 500 x 6 x 8 mm FDA UDI

Identifiers

Primary DI / UDI-DI
E22122551 FDA UDI
FDA Product Code
FRL FDA UDI
GMDN Term
Dental material application tool, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.5300 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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Dental material application tool, single-use

Pele Tim by VOCO GmbH — Class I — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Dental material application tool, single-use.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
VOCO GmbH

Sources (2)

  • FDA UDI 4039bc1f-dc19-485e-85c0-e8fa971153b3 34 fields · synced Jun 19, 2026
  • EUDAMED 1 fields · synced Jun 4, 2026