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Novae

FDA UDI

Class I (US FDA UDI)

by Soc Etudes Recherches Fabrication

Identity

Trade Name
NOVAE FDA UDI
Generic Name
Acetabular orthopaedic reamer FDA UDI
Model / Reference
FT 63 FDA UDI

Identifiers

Primary DI / UDI-DI
03662200013111 FDA UDI
FDA Product Code
HWE FDA UDI
GMDN Term
Acetabular orthopaedic reamer 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

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: Acetabular orthopaedic reamer

Novae by Soc Etudes Recherches Fabrication — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Acetabular orthopaedic reamer.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI e5ae2618-4bd3-43a2-a6e5-468f714ddded 32 fields · synced Jun 1, 2026