Identity
- Trade Name
- RAPORT™ KIT FDA UDI
- Generic Name
- Suture/ligature tightener, single-use FDA UDI
- Device Name
- RAPORT™ KIT RP-75™ FDA UDI
- Model / Reference
- 081730 FDA UDI
- Description
- RAPORT™ KIT RP-75™ FDA UDI
Identifiers
- Catalog Number
- 081730 FDA UDI
- Primary DI / UDI-DI
- 00850012846468 FDA UDI
- FDA Product Code
- MDM FDA UDI
- GMDN Term
- Suture/ligature tightener, single-use FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4800 FDA UDI
- Commercial Distribution
- 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
No
FDA UDI
Combination Product
No
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
Yes
FDA UDI
Category: Suture/ligature tightener, single-use
Raport™ Kit by LSI Solutions, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Suture/ligature tightener, single-use.
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- RAPORT™ — LSI Solutions, Inc. · Class I
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
- LSI Solutions, Inc.
Sources (1)
- FDA UDI 2bd9a6f1-aff4-4d65-8cb1-56ff256d1672 35 fields · synced May 30, 2026