Symmetry Antrum

FDA UDI

Class I (US FDA UDI)

by Symmetry Surgical Inc.

Identity

Trade Name: Symmetry Antrum FDA UDI
Generic Name: Skin-coring punch, reusable FDA UDI
Device Name: Symmetry® Punch, Antrum, 45° Forward Cutting, 4 mm x 5 mm, 8 1/4 in FDA UDI
Model / Reference: 63-7615 FDA UDI
Description: Symmetry® Punch, Antrum, 45° Forward Cutting, 4 mm x 5 mm, 8 1/4 in FDA UDI

Identifiers

Catalog Number: 63-7615 FDA UDI
Primary DI / UDI-DI: 00887482119204 FDA UDI
FDA Product Code: KAW FDA UDI
GMDN Term: Skin-coring punch, reusable FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 874.4420 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size: Width — 4 Millimeter FDA UDI
Depth — 5 Millimeter FDA UDI
Angle — 45 degree FDA UDI
Length — 8.25 Inch FDA UDI

Category: Skin-coring punch, reusable

Symmetry Antrum by Symmetry Surgical Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Symmetry Surgical Inc.

Sources (1)

FDA UDI fa37bdb5-1ecb-449b-bec4-835927eb3177 36 fields · synced May 30, 2026