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Fixed Head Reamer, Ø10mm

FDA UDI

Class I (US FDA UDI)

by I.T.S. GmbH

Identity

Trade Name
Fixed Head Reamer, Ø10mm FDA UDI
Generic Name
Medullary canal orthopaedic reamer, rigid FDA UDI
Device Name
Fixed Head Reamer, Ø10mm FDA UDI
Model / Reference
1UI224A FDA UDI
Description
Fixed Head Reamer, Ø10mm FDA UDI

Identifiers

Catalog Number
1UI224A FDA UDI
Primary DI / UDI-DI
09120116978121 FDA UDI
FDA Product Code
HWE FDA UDI
GMDN Term
Medullary canal orthopaedic reamer, rigid 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

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

No

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: Medullary canal orthopaedic reamer, rigid

Fixed Head Reamer, Ø10mm by I.T.S. GmbH — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Medullary canal orthopaedic reamer, rigid.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
I.T.S. GmbH

Sources (1)

  • FDA UDI 15c90919-686f-46de-a157-f939a672e035 35 fields · synced Jun 8, 2026