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HySolate

FDA UDI

Class I (US FDA UDI)

by Dent4You AG

Identity

Trade Name
HySolate FDA UDI
Generic Name
Rubber dam, non-latex FDA UDI
Device Name
Sample Flexi dam non latex blue FDA UDI
Model / Reference
H00725 FDA UDI
Description
Sample Flexi dam non latex blue FDA UDI

Identifiers

Primary DI / UDI-DI
07630392910972 FDA UDI
FDA Product Code
EIE FDA UDI
GMDN Term
Rubber dam, non-latex FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.6300 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Rubber dam, non-latex

HySolate by Dent4You AG — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Rubber dam, non-latex.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Dent4You AG

Sources (1)

  • FDA UDI 6b265e12-3100-4034-9e34-a4ba6703c3ef 34 fields · synced May 31, 2026