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Reamer Adapter OTD

FDA UDI

Class II (US FDA UDI)

by Ortoma AB (Publ)

Identity

Trade Name
Reamer Adapter OTD FDA UDI
Generic Name
Electromagnetic/optical surgical navigation device tracking system FDA UDI
Model / Reference
1003 FDA UDI

Identifiers

Catalog Number
30-157 FDA UDI
Primary DI / UDI-DI
07350137520081 FDA UDI
510(k) Number
K232140 FDA UDI
FDA Product Code
OLO FDA UDI
GMDN Term
Electromagnetic/optical surgical navigation device tracking system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.4560 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

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

Reamer Adapter OTD by Ortoma AB (Publ) — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Ortoma AB (Publ)

Sources (1)

  • FDA UDI e498331c-7b2a-406d-9772-1980ce2879dc 34 fields · synced Jun 1, 2026