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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
Sponge bowl, reusable FDA UDI
Device Name
Basin, Emesis, 10 oz, 6 5/8 in FDA UDI
Model / Reference
6 FDA UDI
Description
Basin, Emesis, 10 oz, 6 5/8 in FDA UDI

Identifiers

Catalog Number
6 FDA UDI
Primary DI / UDI-DI
00887482106860 FDA UDI
FDA Product Code
FNY FDA UDI
GMDN Term
Sponge bowl, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6730 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

Dimensions & Sizes

Size
Length — 6.625 Inch FDA UDI
Total Volume — 10 Fluid Ounce FDA UDI

Category: Sponge bowl, reusable

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

Similar devices

Also classified as Sponge bowl, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 703f9a5a-01e9-4152-b178-7203bd851caf 36 fields · synced Jun 7, 2026