Identity
- Trade Name
- DISSECTOR FDA UDI
- Generic Name
- Paranasal sinus curette FDA UDI
- Device Name
- ENDOSCOPIC, NO. 1 FDA UDI
- Model / Reference
- 38-550-01-07 FDA UDI
- Description
- ENDOSCOPIC, NO. 1 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00888118062536 FDA UDI
- FDA Product Code
- GZX FDA UDI
- GMDN Term
- Paranasal sinus curette FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 882.4525 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
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Paranasal sinus curette
Dissector by KLS-Martin L.P. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Paranasal sinus curette.
- Bausch + Lomb — Bausch & Lomb, Inc. · Class I
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- Sklar — Sklar Corporation · Class I
- STOMA® — Storz am Mark GmbH · Class I
- SINUS CURETTE MB 2 HD D/E — W.H. Holden, Inc. · Class I
- J & J INSTRUMENTS — J&J Instruments, LLC · Class I
- Integra® — Integra LifeSciences Production Corporation · Class I
- V. Mueller — STERIS CORPORATION · 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
- KLS-Martin L.P.
Sources (1)
- FDA UDI 1e4eb9b1-4ede-4659-9065-c1a67049e444 34 fields · synced May 30, 2026