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Symmetry Cooley

FDA UDI

Class II (US FDA UDI)

by Symmetry Surgical Inc.

Identity

Trade Name
Symmetry Cooley FDA UDI
Generic Name
Fixed-diameter cervical dilator, reusable FDA UDI
Device Name
Symmetry® Dilator; Cooley; (6/st) FDA UDI
Model / Reference
55-7001 FDA UDI
Description
Symmetry® Dilator; Cooley; (6/st) FDA UDI

Identifiers

Catalog Number
55-7001 FDA UDI
Primary DI / UDI-DI
00887482141755 FDA UDI
FDA Product Code
DWP FDA UDI
GMDN Term
Fixed-diameter cervical dilator, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.4475 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

Category: Fixed-diameter cervical dilator, reusable

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

Similar devices

Also classified as Fixed-diameter cervical dilator, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 6cc02ac9-e792-449d-a4aa-fca4f7671dc4 35 fields · synced Jun 8, 2026