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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
Bowl, Sponge, 7 1/8 x 2 3/4, 48 oz FDA UDI
Model / Reference
148-0 FDA UDI
Description
Bowl, Sponge, 7 1/8 x 2 3/4, 48 oz FDA UDI

Identifiers

Catalog Number
148-0 FDA UDI
Primary DI / UDI-DI
00887482055472 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
Height — 2.75 Inch 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 ff51c12b-17fe-47f6-adab-df654eef73db 36 fields · synced May 31, 2026