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Probes Simple Ended

FDA UDI

Class I (US FDA UDI)

by Maillefer Instruments Holding Sàrl

Identity

Trade Name
PROBES SIMPLE ENDED FDA UDI
Generic Name
Dental surgical probe, reusable FDA UDI
Device Name
N/A FDA UDI
Model / Reference
B009300002100 FDA UDI
Description
N/A FDA UDI

Identifiers

Catalog Number
B009300002100 FDA UDI
Primary DI / UDI-DI
J003B0093000021001 FDA UDI
FDA Product Code
EIX FDA UDI
GMDN Term
Dental surgical probe, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4565 FDA UDI
Commercial Distribution
Not 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

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

Probes Simple Ended by Maillefer Instruments Holding Sàrl — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 0f504ffc-919b-4d06-a336-c54c1c27e76c 36 fields · synced Jun 9, 2026