← Back to catalogue

DryShield

FDA UDI

Class I (US FDA UDI)

by Solmetex, LLC

Identity

Trade Name
DryShield FDA UDI
Generic Name
Dental suction system FDA UDI
Device Name
Mouthpiece - Autoclave - SMALL - 4 Pack FDA UDI
Model / Reference
BMD DS-MPS-003 FDA UDI
Description
Mouthpiece - Autoclave - SMALL - 4 Pack FDA UDI

Identifiers

Primary DI / UDI-DI
00850045062088 FDA UDI
FDA Product Code
DYN FDA UDI
GMDN Term
Dental suction system FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.6640 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

No

FDA UDI

Over-the-Counter

Yes

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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Dental suction system

DryShield by Solmetex, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental suction system.

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
Solmetex, LLC

Sources (1)

  • FDA UDI e86e5c72-2733-4b6f-8073-742120a32ba9 35 fields · synced Jun 9, 2026