Identity
- Trade Name
- Curaplex FDA UDI
- Generic Name
- Rigid intubation laryngoscope, reusable FDA UDI
- Device Name
- *Custom* Epi Kit Replacement Parts FDA UDI
- Model / Reference
- 8600-EPIKITRP FDA UDI
- Description
- *Custom* Epi Kit Replacement Parts FDA UDI
Identifiers
- Catalog Number
- 8600-EPIKITRP FDA UDI
- Primary DI / UDI-DI
- 00812277033502 FDA UDI
- FDA Product Code
- CCW FDA UDI
- GMDN Term
- Rigid intubation laryngoscope, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 868.5540 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
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
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Rigid intubation laryngoscope, reusable
Curaplex by Bound Tree Medical, Llc — Class I — 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 I | Pending data |
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Manufacturer
- Manufacturer
- Bound Tree Medical, Llc
Sources (1)
- FDA UDI 95a8a380-d749-4b0a-a218-81620060ac59 34 fields · synced May 30, 2026