Identity
- Trade Name
- Racord Two Retraction Cord 10/2 FDA UDI
- Generic Name
- Gingival retraction cord, medicated FDA UDI
- Device Name
- Twisted Gingival Retraction Cord with Epinephrine and Zinc Phenolsulfonate, 72 inches, size 10/2 FDA UDI
- Model / Reference
- 07820 FDA UDI
- Description
- Twisted Gingival Retraction Cord with Epinephrine and Zinc Phenolsulfonate, 72 inches, size 10/2 FDA UDI
Identifiers
- Catalog Number
- 07820 FDA UDI
- Primary DI / UDI-DI
- 00310866000596 FDA UDI
- FDA Product Code
- MVL FDA UDI
- GMDN Term
- Gingival retraction cord, medicated FDA UDI
Classification
- Device Class
- U FDA UDI
- Commercial Distribution
- Not 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
Yes
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
Racord Two Retraction Cord 10/2 by Pascal Company, Inc. — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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
- Pascal Company, Inc.
Sources (1)
- FDA UDI 882a2725-7b4d-4e8b-81ef-2e78cb5b68cd 37 fields · synced May 31, 2026