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Synth™ Vrt

FDA UDI

Class I (US FDA UDI)

by Imedicom Co., Ltd.

Identity

Trade Name
SYNTH™ VRT FDA UDI
Generic Name
Orthopaedic cement preparation/delivery kit FDA UDI
Device Name
HC Biologics Private Label(11G-100) FDA UDI
Model / Reference
SYNTH-V100 FDA UDI
Description
HC Biologics Private Label(11G-100) FDA UDI

Identifiers

Primary DI / UDI-DI
08800038055674 FDA UDI
FDA Product Code
OAR FDA UDI
GMDN Term
Orthopaedic cement preparation/delivery kit FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4200 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Orthopaedic cement preparation/delivery kit

Synth™ Vrt by Imedicom Co., Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic cement preparation/delivery kit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Imedicom Co., Ltd.

Sources (1)

  • FDA UDI 9ef85c00-b2cc-4a35-9c7a-1bd7962e97e6 33 fields · synced Jun 8, 2026