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Symmetry Love-Gruenwald

FDA UDI

Class II (US FDA UDI)

by Symmetry Surgical Inc.

Identity

Trade Name
Symmetry Love-Gruenwald FDA UDI
Generic Name
Spinal rongeur FDA UDI
Device Name
Symmetry® Rongeur; Del IVD; Angled Down; 3 mm x 10 mm FDA UDI
Model / Reference
57-2332 FDA UDI
Description
Symmetry® Rongeur; Del IVD; Angled Down; 3 mm x 10 mm FDA UDI

Identifiers

Catalog Number
57-2332 FDA UDI
Primary DI / UDI-DI
00887482095140 FDA UDI
FDA Product Code
HAE FDA UDI
GMDN Term
Spinal rongeur FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.4840 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
Width — 3 Millimeter FDA UDI
Depth — 10 Millimeter FDA UDI

Category: Spinal rongeur

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

Similar devices

Also classified as Spinal rongeur.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 0aa98ab1-076d-432c-916a-bbbe9c182273 36 fields · synced May 30, 2026