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Symmetry Surgical

FDA UDI

Class I (US FDA UDI)

by Symmetry Surgical Inc.

Identity

Trade Name
Symmetry Surgical FDA UDI
Generic Name
Skin marking guide, single-use FDA UDI
Device Name
Symmetry® Marker, Symmetry Surgical, Single Use, (36/bx) FDA UDI
Model / Reference
43-1030 FDA UDI
Description
Symmetry® Marker, Symmetry Surgical, Single Use, (36/bx) FDA UDI

Identifiers

Primary DI / UDI-DI
00887482012819 FDA UDI
FDA Product Code
FZZ FDA UDI
GMDN Term
Skin marking guide, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4660 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Skin marking guide, single-use

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

Similar devices

Also classified as Skin marking guide, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Symmetry Surgical Inc.

Sources (1)

  • FDA UDI f88bbfc8-0427-42ef-849b-fcc520a44ec0 34 fields · synced May 30, 2026