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Breast Reduction Marker

FDA UDI

Class I (US FDA UDI)

by Sontec Instruments, Inc.

Identity

Trade Name
BREAST REDUCTION MARKER FDA UDI
Generic Name
Skin marking guide, reusable FDA UDI
Device Name
BREAST REDUCTION MARKER MEDIUM SIZE FDA UDI
Model / Reference
475-916M FDA UDI
Description
BREAST REDUCTION MARKER MEDIUM SIZE FDA UDI

Identifiers

Catalog Number
475-916M FDA UDI
Primary DI / UDI-DI
00192896098572 FDA UDI
FDA Product Code
MDM FDA UDI
GMDN Term
Skin marking guide, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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

Category: Skin marking guide, reusable

Breast Reduction Marker by Sontec Instruments, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Skin marking guide, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 217fd07f-4942-4e7c-9aef-3a25717a3cba 35 fields · synced May 30, 2026