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Attachment Adapter Fix OT

FDA UDIEUDAMED

Class II (US FDA UDI)

Ref 30-156

by Ortoma AB (Publ)

Identity

Trade Name
OTS™ Aufsatzadapter Fix OT EUDAMED
Attachment Adapter Fix OT FDA UDI
Generic Name
Electromagnetic/optical surgical navigation device tracking system FDA UDI
Device Name
OTS Reusable Instruments EUDAMED
Model / Reference
30-156 EUDAMED
1002 FDA UDI

Identifiers

Catalog Number
30-156 FDA UDI
Primary DI / UDI-DI
07350137520074 EUDAMEDFDA UDI
Basic UDI-DI
735013752OTSInstrument39 EUDAMED
Direct Marketing DI
07350137520074 EUDAMED
510(k) Number
K232140 FDA UDI
FDA Product Code
OLO FDA UDI
EMDN Code
Z12011401 SURGICAL NAVIGATION SYSTEM EUDAMED
GMDN Term
Electromagnetic/optical surgical navigation device tracking system FDA UDI

Classification

Device Class
Class I EUDAMED
Class II FDA UDI
Regulation Number
882.4560 FDA UDI
Market of Registration
Sweden 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

No

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: Electromagnetic/optical surgical navigation device tracking system

Attachment Adapter Fix OT by Ortoma AB (Publ) — Class II — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Electromagnetic/optical surgical navigation device tracking system.

Cleared under the same submission

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Ortoma AB (Publ)

Sources (2)

  • FDA UDI c80b3715-f13c-4fac-bb26-f03ef63c3ed9 34 fields · synced Jul 9, 2026
  • EUDAMED 69306640-e8ad-44dc-b82f-49d1fbfb20e4 61 fields · synced Jul 9, 2026