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Eberle

FDA UDI

Class II (US FDA UDI)

by Eberle GmbH & Co. KG

Identity

Trade Name
EBERLE FDA UDI
Generic Name
Arthroscopic shaver system blade, reusable FDA UDI
Device Name
Drill chuck adapter, high-power, 0.7-7.4 mm FDA UDI
Model / Reference
913019 FDA UDI
Description
Drill chuck adapter, high-power, 0.7-7.4 mm FDA UDI

Identifiers

Catalog Number
913019 FDA UDI
Primary DI / UDI-DI
04050052023362 FDA UDI
FDA Product Code
HRX FDA UDI
GMDN Term
Arthroscopic shaver system blade, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.1100 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Arthroscopic shaver system blade, reusable

Eberle by Eberle GmbH & Co. KG — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Arthroscopic shaver system blade, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Eberle GmbH & Co. KG

Sources (1)

  • FDA UDI 6ba6f1be-1790-4b84-96ce-018c1964edd8 34 fields · synced Jun 6, 2026