← Back to catalogue

Attachment Adapter Twin OT

FDA UDIEUDAMED

Class II (US FDA UDI)

Ref 30-142

by Ortoma AB (Publ)

Identity

Trade Name
OTS™ Aufsatzadapter Twin OT EUDAMED
Attachment Adapter Twin OT FDA UDI
Generic Name
Electromagnetic/optical surgical navigation device tracking system FDA UDI
Device Name
OTS Reusable Instruments EUDAMED
Model / Reference
30-142 EUDAMED
1006 FDA UDI

Identifiers

Catalog Number
30-142 FDA UDI
Primary DI / UDI-DI
07350137520968 EUDAMEDFDA UDI
Basic UDI-DI
735013752OTSInstrument39 EUDAMED
Direct Marketing DI
07350137520968 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 Twin 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

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

Manufacturer

Manufacturer
Ortoma AB (Publ)

Sources (2)

  • FDA UDI 30b08fc6-6ca8-462b-bf71-d6b15d4eecb7 34 fields · synced Jun 18, 2026
  • EUDAMED 42f72e17-df52-4df3-8a5d-53c1c7ed9949 61 fields · synced Jun 18, 2026