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SurgiMac

FDA UDI

Class I (US FDA UDI)

by Surgimac LLC

Identity

Trade Name
SurgiMac FDA UDI
Generic Name
Spring-loaded dental mallet FDA UDI
Device Name
Morrell-Type Crown Remover FDA UDI
Model / Reference
13-1176 FDA UDI
Description
Morrell-Type Crown Remover FDA UDI

Identifiers

Catalog Number
13-1176 FDA UDI
Primary DI / UDI-DI
D105SKU1311760 FDA UDI
FDA Product Code
EIS FDA UDI
GMDN Term
Spring-loaded dental mallet 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

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Spring-loaded dental mallet

SurgiMac by Surgimac LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Spring-loaded dental mallet.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Surgimac LLC

Sources (1)

  • FDA UDI 7783169f-a7c3-4f55-9e1c-7a5080e39a4a 34 fields · synced May 30, 2026