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Ennovate

FDA UDIEUDAMED

Class I (US FDA UDI)

Ref SZ351R

by Aesculap, Inc.

Identity

Trade Name
Ennovate® EUDAMED
ENNOVATE FDA UDI
Generic Name
Orthopaedic prosthesis implantation positioning instrument, reusable FDA UDI
Device Name
ENNOVATE implant. instrument Ir EUDAMED
ENNOVATE PEDICLE PREPARATOR FDA UDI
Model / Reference
SZ351R EUDAMEDFDA UDI
Description
ENNOVATE PEDICLE PREPARATOR FDA UDI

Identifiers

Catalog Number
SZ351R FDA UDI
Primary DI / UDI-DI
04046964700552 EUDAMEDFDA UDI
Basic UDI-DI
4039239000000350ZS EUDAMED
Direct Marketing DI
04046964700552 EUDAMED
FDA Product Code
LXH FDA UDI
EMDN Code
L091199 ORTHOPAEDIC PROSTHETICS INSTRUMENTS, REUSABLE - OTHER EUDAMED
GMDN Term
Orthopaedic prosthesis implantation positioning instrument, reusable FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
888.4540 FDA UDI
Market of Registration
Germany EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

Yes

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

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

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Orthopaedic prosthesis implantation positioning instrument, reusable

Ennovate by Aesculap, Inc. — Class I — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic prosthesis implantation positioning instrument, reusable.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Aesculap, Inc.

Sources (2)

  • FDA UDI 35b6340b-704f-4599-8cd7-51909f60ab72 35 fields · synced Oct 8, 2026
  • EUDAMED 29a63b05-4ef5-4828-a608-d3751f3467ea 61 fields · synced Oct 8, 2026