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Symmetry Boucheron

FDA UDI

Class I (US FDA UDI)

by Symmetry Surgical Inc.

Identity

Trade Name
Symmetry Boucheron FDA UDI
Generic Name
Gelfoam punch FDA UDI
Device Name
Symmetry® Speculum, Boucheron, Chrome Plated, Round, Large, 5.5 mm To 9.0 mm, (4/st) FDA UDI
Model / Reference
61-0905 FDA UDI
Description
Symmetry® Speculum, Boucheron, Chrome Plated, Round, Large, 5.5 mm To 9.0 mm, (4/st) FDA UDI

Identifiers

Catalog Number
61-0905 FDA UDI
Primary DI / UDI-DI
00887482145845 FDA UDI
FDA Product Code
EPY FDA UDI
GMDN Term
Gelfoam punch FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.1800 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
Circumference — 5.5 Millimeter FDA UDI
Circumference — 9 Millimeter FDA UDI

Category: Gelfoam punch

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

Similar devices

Also classified as Gelfoam punch.

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 d856cb8d-948d-4d35-84c4-cea20d748153 36 fields · synced May 30, 2026