← Back to catalogue

Symmetry Rhoton®

FDA UDI

Class I (US FDA UDI)

by Symmetry Surgical Inc.

Identity

Trade Name
Symmetry Rhoton® FDA UDI
Generic Name
Body aspiration needle, reusable FDA UDI
Device Name
Rhoton® Needle, Straight, Semi-Sharp, 7 1/2 in FDA UDI
Model / Reference
58-6040 FDA UDI
Description
Rhoton® Needle, Straight, Semi-Sharp, 7 1/2 in FDA UDI

Identifiers

Catalog Number
58-6040 FDA UDI
Primary DI / UDI-DI
00887482103593 FDA UDI
FDA Product Code
HAS FDA UDI
GMDN Term
Body aspiration needle, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
882.4650 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 — 7.5 Inch FDA UDI

Category: Body aspiration needle, reusable

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

Similar devices

Also classified as Body aspiration needle, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 03d487b9-2380-4a88-92f8-941e4b194295 36 fields · synced Jun 1, 2026