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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
General-purpose surgical sponge FDA UDI
Device Name
Secto® Sponge, Bulk Tonsil, Medium, Non-Sterile Product (100 units / 5 sponges each) FDA UDI
Model / Reference
24-5511 FDA UDI
Description
Secto® Sponge, Bulk Tonsil, Medium, Non-Sterile Product (100 units / 5 sponges each) FDA UDI

Identifiers

Primary DI / UDI-DI
00887482002285 FDA UDI
FDA Product Code
GDY FDA UDI
GMDN Term
General-purpose surgical sponge FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4450 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: General-purpose surgical sponge

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

Similar devices

Also classified as General-purpose surgical sponge.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 5d3ea8a6-5680-45e9-ab51-08d1d706cd1f 34 fields · synced May 30, 2026