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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
Immersion basket FDA UDI
Model / Reference
900312 FDA UDI
Description
Immersion basket FDA UDI

Identifiers

Catalog Number
900312 FDA UDI
Primary DI / UDI-DI
04050052027971 FDA UDI
FDA Product Code
LHX FDA UDI
GMDN Term
Arthroscopic shaver system blade, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.5800 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

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 62c3fb83-25c7-46e3-9ea1-2cff513a1e58 34 fields · synced May 30, 2026