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TAPESTRY RC Biointegrative Implant System
FDA UDIClass I (US FDA UDI)
by Embody, Inc.
Identity
- Trade Name
- TAPESTRY RC Biointegrative Implant System FDA UDI
- Generic Name
- Arthroscopic surgical procedure kit, non-medicated, single-use FDA UDI
- Device Name
- Convenience Kit FDA UDI
- Model / Reference
- TR-3030-L6 FDA UDI
- Description
- Convenience Kit FDA UDI
Identifiers
- Catalog Number
- TR-3030-L6 FDA UDI
- Primary DI / UDI-DI
- 00810063820237 FDA UDI
- FDA Product Code
- OJH FDA UDI
- GMDN Term
- Arthroscopic surgical procedure kit, non-medicated, single-use FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4800 FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
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
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
MR Safe FDA UDI
TAPESTRY RC Biointegrative Implant System by Embody, Inc. — Class I — 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 I | Pending data |
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Manufacturer
- Manufacturer
- Embody, Inc.
Sources (1)
- FDA UDI a198b45a-b050-4250-8adb-90721b09aa31 35 fields · synced May 30, 2026