← Back to catalogue

Spacer

FDA UDI

Class II (US FDA UDI)

by Vericom Co., Ltd.

Identity

Trade Name
Spacer FDA UDI
Generic Name
Temporary dental crown/bridge FDA UDI
Device Name
Light-curing Temporary Filling Material ; Spacer Blue 3g x 3 syringes FDA UDI
Model / Reference
SP103-B000 FDA UDI
Description
Light-curing Temporary Filling Material ; Spacer Blue 3g x 3 syringes FDA UDI

Identifiers

Primary DI / UDI-DI
08809254451864 FDA UDI
FDA Product Code
EBF FDA UDI
GMDN Term
Temporary dental crown/bridge FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3690 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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Temporary dental crown/bridge

Spacer by Vericom Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Temporary dental crown/bridge.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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

Manufacturer

Manufacturer
Vericom Co., Ltd.

Sources (1)

  • FDA UDI 5c38c1a0-cd2d-4b4a-984f-6ea4925367c7 35 fields · synced Jun 1, 2026