← Back to catalogue

Ultrapower

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref 7020-019

by Conmed Corporation

Identity

Trade Name
ULTRAPOWER EUDAMEDFDA UDI
Generic Name
Surgical instrument guard, reusable FDA UDI
Device Name
Orthopedic, Non-active, Guard, Ultrapower EUDAMED
ULTRAPOWER NEURO GUARD, LONG FDA UDI
Model / Reference
7020-019 EUDAMED
00702001900 FDA UDI
Description
ULTRAPOWER NEURO GUARD, LONG FDA UDI

Identifiers

Catalog Number
7020-019 FDA UDI
Primary DI / UDI-DI
10845854023938 EUDAMEDFDA UDI
Basic UDI-DI
B-10845854023938 EUDAMED
FDA Product Code
GET FDA UDI
EMDN Code
L090999 ORTHOPAEDIC SURGERY CUTTING INSTRUMENTS, REUSABLE - OTHER EUDAMED
GMDN Term
Surgical instrument guard, reusable FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class I FDA UDI
Regulation Number
878.4820 FDA UDI
Market of Registration
Belgium EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

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

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Bone cutting forceps, reusable

Ultrapower by Conmed Corporation — Class IIa — MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bone cutting forceps, reusable.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDD

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Conmed Corporation
EUDAMED SRN
US-MF-000012663
Authorised Representative
MDSS GmbH DE-AR-000005430

Sources (2)

  • EUDAMED 114c575f-9ecd-4b3b-a56b-4a25b31f3713 61 fields · synced May 30, 2026
  • FDA UDI cc6d5368-1dc8-4927-a731-a966b29066cd 35 fields · synced May 30, 2026