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Symmetry Surgical

FDA UDI

Class II (US FDA UDI)

by Symmetry Surgical Inc.

Identity

Trade Name
Symmetry Surgical FDA UDI
Generic Name
Laparoscopic access cannula, reusable FDA UDI
Device Name
Symmetry® Sleeve; Reducer; 10 mm FDA UDI
Model / Reference
90-5035 FDA UDI
Description
Symmetry® Sleeve; Reducer; 10 mm FDA UDI

Identifiers

Catalog Number
90-5035 FDA UDI
Primary DI / UDI-DI
00887482129777 FDA UDI
510(k) Number
K040855 FDA UDI
FDA Product Code
GEI FDA UDI
GMDN Term
Laparoscopic access cannula, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4400 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

No

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

No

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

Dimensions & Sizes

Size
Length — 10 Millimeter FDA UDI

Category: Laparoscopic access cannula, reusable

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

Similar devices

Also classified as Laparoscopic access cannula, reusable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 889511e5-86f3-43cb-9320-7e793e40660b 37 fields · synced May 30, 2026