← Back to catalogue

Standard Short Light Wand Only (.187x3)

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 8011-01

by Innomed, Inc.

Identity

Trade Name
Standard Short Light Wand Only (.187x3) EUDAMED
Innomed, Inc. FDA UDI
Generic Name
Endoscopic surgical probe FDA UDI
Device Name
Probe EUDAMED
Standard Short Light Wand Only (.187 x 3) FDA UDI
Model / Reference
8011-01 EUDAMEDFDA UDI
Description
Standard Short Light Wand Only (.187 x 3) FDA UDI

Identifiers

Catalog Number
8011-0 FDA UDI
Primary DI / UDI-DI
00840277126016 EUDAMEDFDA UDI
Basic UDI-DI
8402771INNOPROBE0133 EUDAMED
Direct Marketing DI
00840277126016 EUDAMED
FDA Product Code
HXB FDA UDI
EMDN Code
L0999 ORTHOPAEDIC AND TRAUMATOLOGICAL SURGERY INSTRUMENTS, REUSABLE - OTHER EUDAMED
GMDN Term
Endoscopic surgical probe 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

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

No

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

Standard Short Light Wand Only (.187x3) by Innomed, Inc. — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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

Manufacturer

Manufacturer
Innomed, Inc.
EUDAMED SRN
US-MF-000014761
Authorised Representative
MediMark Europe Sarl. FR-AR-000000182

Sources (2)

  • EUDAMED 1778e647-d483-485b-bf15-d51ce9740b5f 61 fields · synced Jun 18, 2026
  • FDA UDI 24a6b4bd-dc34-46a3-a756-a575c0997e7c 34 fields · synced May 30, 2026