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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
Body aspiration needle, reusable FDA UDI
Device Name
Symmetry® Needle, Aspirator, 22 G, 450 mm FDA UDI
Model / Reference
90-5052L FDA UDI
Description
Symmetry® Needle, Aspirator, 22 G, 450 mm FDA UDI

Identifiers

Catalog Number
90-5052L FDA UDI
Primary DI / UDI-DI
00887482129852 FDA UDI
FDA Product Code
MDM FDA UDI
GMDN Term
Body aspiration needle, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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
Needle Gauge — 22 Gauge FDA UDI
Length — 450 Millimeter FDA UDI

Category: Body aspiration needle, reusable

Symmetry Surgical 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

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Manufacturer

Sources (1)

  • FDA UDI 6855c4c2-db6e-4d4f-8883-a3a41a412773 36 fields · synced Jun 8, 2026