Identity
- Trade Name
- Re-Cord™ Knitted Retraction Cord #1 FDA UDI
- Generic Name
- Gingival retraction cord, medicated FDA UDI
- Device Name
- Gingival retraction cord, non-medicated FDA UDI
- Model / Reference
- 649104 FDA UDI
- Description
- Gingival retraction cord, non-medicated FDA UDI
Identifiers
- Catalog Number
- 649104 FDA UDI
- Primary DI / UDI-DI
- 00359883005726 FDA UDI
- FDA Product Code
- JES FDA UDI
- GMDN Term
- Gingival retraction cord, medicated FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 872.6390 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
No
FDA UDI
Manufacturing Date
No
FDA UDI
Dimensions & Sizes
- Size
- Length — 244 Centimeter FDA UDI
Category: Gingival retraction cord, medicated
Re-Cord™ Knitted Retraction Cord #1 by Den-Mat Holdings, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Gingival retraction cord, medicated.
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- Racellet 3 Pellets — PASCAL COMPANY, INC. · U
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 I | Pending data |
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Manufacturer
- Manufacturer
- Den-Mat Holdings, LLC
Sources (1)
- FDA UDI b596b9a0-6faa-45d4-9427-109f27513fab 37 fields · synced Jun 9, 2026