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Symmetry Atkinson

FDA UDI

Class I (US FDA UDI)

by Symmetry Surgical Inc.

Identity

Trade Name
Symmetry Atkinson FDA UDI
Generic Name
Laparoscopic irrigation cannula FDA UDI
Device Name
Symmetry® Cannula, Atkison Retrobulbar, 25 Gauge FDA UDI
Model / Reference
60-1226 FDA UDI
Description
Symmetry® Cannula, Atkison Retrobulbar, 25 Gauge FDA UDI

Identifiers

Catalog Number
60-1226 FDA UDI
Primary DI / UDI-DI
00887482107720 FDA UDI
FDA Product Code
HMX FDA UDI
GMDN Term
Laparoscopic irrigation cannula FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
886.4350 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

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Laparoscopic irrigation cannula

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

Similar devices

Also classified as Laparoscopic irrigation cannula.

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 96f2f1aa-992e-416e-bbfe-ce1d9a67faee 35 fields · synced Jun 1, 2026