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Symmetry FANSLER

FDA UDI

Class II (US FDA UDI)

by Symmetry Surgical Inc.

Identity

Trade Name
Symmetry FANSLER FDA UDI
Generic Name
Optical proctoscope, reusable FDA UDI
Device Name
Symmetry® Proctoscope; Fansler; 2 1/3 in FDA UDI
Model / Reference
79-5555 FDA UDI
Description
Symmetry® Proctoscope; Fansler; 2 1/3 in FDA UDI

Identifiers

Catalog Number
79-5555 FDA UDI
Primary DI / UDI-DI
00887482030318 FDA UDI
FDA Product Code
GCF FDA UDI
GMDN Term
Optical proctoscope, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1500 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 — 2.3333 Inch FDA UDI

Category: Optical proctoscope, reusable

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

Similar devices

Also classified as Optical proctoscope, reusable.

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 ef642a32-fe30-45db-b947-1ba2148c5cbc 36 fields · synced May 30, 2026