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Angled Handpiece

FDA UDI

Class I (US FDA UDI)

by Elliquence Llc

Identity

Trade Name
Angled Handpiece FDA UDI
Generic Name
Spinal decompression cutting handpiece/endpiece FDA UDI
Model / Reference
16-0100 FDA UDI

Identifiers

Primary DI / UDI-DI
00846338002695 FDA UDI
FDA Product Code
GEY FDA UDI
GMDN Term
Spinal decompression cutting handpiece/endpiece FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4820 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

No

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Spinal decompression cutting handpiece/endpiece

Angled Handpiece by Elliquence Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Spinal decompression cutting handpiece/endpiece.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Elliquence Llc

Sources (1)

  • FDA UDI 2052bf3a-f19a-4635-891d-b3f9e3606030 32 fields · synced May 30, 2026