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Symmetry Hudson

FDA UDI

Class II (US FDA UDI)

by Symmetry Surgical Inc.

Identity

Trade Name
Symmetry Hudson FDA UDI
Generic Name
Biopsy drill bit FDA UDI
Device Name
Symmetry® Burr; Hudson; 22 mm FDA UDI
Model / Reference
15-1008 FDA UDI
Description
Symmetry® Burr; Hudson; 22 mm FDA UDI

Identifiers

Catalog Number
15-1008 FDA UDI
Primary DI / UDI-DI
00887482000342 FDA UDI
FDA Product Code
HBG FDA UDI
GMDN Term
Biopsy drill bit FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.4300 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: Biopsy drill bit

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

Similar devices

Also classified as Biopsy drill bit.

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 a106b82c-643c-4210-8758-6a2e884a2c0d 36 fields · synced Jun 6, 2026