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Symmetry Erich

FDA UDI

Class I (US FDA UDI)

by Symmetry Surgical Inc.

Identity

Trade Name
Symmetry Erich FDA UDI
Generic Name
Maxillofacial bone wire/bar FDA UDI
Device Name
Symmetry® Bars, Erich Arch Bar, (1 Meter Roll) FDA UDI
Model / Reference
68-1505 FDA UDI
Description
Symmetry® Bars, Erich Arch Bar, (1 Meter Roll) FDA UDI

Identifiers

Catalog Number
68-1505 FDA UDI
Primary DI / UDI-DI
00887482035252 FDA UDI
FDA Product Code
LXH FDA UDI
GMDN Term
Maxillofacial bone wire/bar FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

Yes

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

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Maxillofacial bone wire/bar

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

Similar devices

Also classified as Maxillofacial bone wire/bar.

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 7d5d0427-6bda-428c-a111-457c0e1a49a3 35 fields · synced May 30, 2026