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Mi1210 Implant Template

FDA UDI

Class III (US FDA UDI)

by Med-El Elektromedizinische Geräte Gesellschaft m.b.H.

Identity

Trade Name
Mi1210 Implant Template FDA UDI
Generic Name
Surgical implant template, single-use FDA UDI
Device Name
Single-Use Surgical Tool FDA UDI
Model / Reference
33056 FDA UDI
Description
Single-Use Surgical Tool FDA UDI

Identifiers

Primary DI / UDI-DI
09008737330569 FDA UDI
PMA Number
P000025 FDA UDI
FDA Product Code
MCM FDA UDI
GMDN Term
Surgical implant template, single-use FDA UDI

Classification

Device Class
Class III FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Surgical implant template, single-use

Mi1210 Implant Template by Med-El Elektromedizinische Geräte Gesellschaft m.b.H. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical implant template, single-use.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI d98fc7a1-5aa0-4338-8f15-8ef86a8be8b2 36 fields · synced May 30, 2026