Identity
- Trade Name
- Dryz™ FDA UDI
- Generic Name
- Gingival retraction cord, non-medicated FDA UDI
- Device Name
- DryZ® Syringe Gingival Retraction Paste Sample (Contains; 1- Syringe & 2-Tips) with Japanese Instructions FDA UDI
- Model / Reference
- S184SPJ FDA UDI
- Description
- DryZ® Syringe Gingival Retraction Paste Sample (Contains; 1- Syringe & 2-Tips) with Japanese Instructions FDA UDI
Identifiers
- Catalog Number
- S184SPJ FDA UDI
- Primary DI / UDI-DI
- 00810000525355 FDA UDI
- FDA Product Code
- MVL FDA UDI
- GMDN Term
- Gingival retraction cord, non-medicated FDA UDI
Classification
- Device Class
- U 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
No
FDA UDI
Category: Gingival retraction cord, non-medicated
Dryz™ by Parkell, Inc. — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class U | Pending data |
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Manufacturer
- Manufacturer
- Parkell, Inc.
Sources (1)
- FDA UDI ae1811c1-48c9-4d74-869c-dbd8b9f105a1 36 fields · synced May 30, 2026