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EmbedMed

FDA UDI

Class II (US FDA UDI)

by 3D Lifeprints UK , Ltd.

Identity

Trade Name
EmbedMed FDA UDI
Generic Name
Custom-made organ/bone anatomy model FDA UDI
Device Name
Patient-specific, Maxillofacial Anatomical Model, Non-sterile FDA UDI
Model / Reference
CMFAMNS FDA UDI
Description
Patient-specific, Maxillofacial Anatomical Model, Non-sterile FDA UDI

Identifiers

Primary DI / UDI-DI
00860009815704 FDA UDI
FDA Product Code
LLZ FDA UDI
DZJ FDA UDI
GMDN Term
Custom-made organ/bone anatomy model FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.2050 FDA UDI
872.4120 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Safe FDA UDI

Category: Custom-made organ/bone anatomy model

EmbedMed by 3D Lifeprints UK , Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Custom-made organ/bone anatomy model.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 041665c4-9800-481c-b067-ce8adc64c926 33 fields · synced May 30, 2026