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Dry Rite Drying Agent

FDA UDI

Class II (US FDA UDI)

by Pulpdent Corporation

Identity

Trade Name
DRY RITE DRYING AGENT FDA UDI
Generic Name
Medical device cleaning agent FDA UDI
Device Name
KIT: 4 x 1.2 mL syringes + 8 pre-bent dropper tips FDA UDI
Model / Reference
DRY FDA UDI
Description
KIT: 4 x 1.2 mL syringes + 8 pre-bent dropper tips FDA UDI

Identifiers

Primary DI / UDI-DI
D701SDRY2 FDA UDI
510(k) Number
K896654 FDA UDI
FDA Product Code
EBF FDA UDI
GMDN Term
Medical device cleaning agent 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

Yes

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

No

FDA UDI

Dimensions & Sizes

Size
Total Volume — 1.2 Milliliter FDA UDI

Category: Medical device cleaning agent

Dry Rite Drying Agent by Pulpdent Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Medical device cleaning agent.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 3849449c-65c2-4d63-8621-bb9971102b89 35 fields · synced Jun 9, 2026