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Miniature Blumenthal Rongeur

FDA UDI

Class I (US FDA UDI)

by Sontec Instruments, Inc.

Identity

Trade Name
MINIATURE BLUMENTHAL RONGEUR FDA UDI
Generic Name
Dental rongeur FDA UDI
Device Name
MINIATURE BLUMENTHAL RONGEUR TAPERED DELICATE ANGLED JAW FDA UDI
Model / Reference
315-500M FDA UDI
Description
MINIATURE BLUMENTHAL RONGEUR TAPERED DELICATE ANGLED JAW FDA UDI

Identifiers

Catalog Number
315-500M FDA UDI
Primary DI / UDI-DI
00192896027213 FDA UDI
FDA Product Code
EMH FDA UDI
GMDN Term
Dental rongeur FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4565 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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Length — 4.5 Inch FDA UDI

Category: Dental rongeur

Miniature Blumenthal Rongeur by Sontec Instruments, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental rongeur.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 05a2f888-70e9-4685-9256-1d9fa3dea8dc 36 fields · synced May 30, 2026