Identity
- Trade Name
- Gyrus ACMI FDA UDI
- Generic Name
- Resectoscope FDA UDI
- Device Name
- RESECTOSCOPE KIT (P) 3 ASSYS FDA UDI
- Model / Reference
- 714720 FDA UDI
- Description
- RESECTOSCOPE KIT (P) 3 ASSYS FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00821925009165 FDA UDI
- 510(k) Number
- K990628 FDA UDI
- FDA Product Code
- FDS FDA UDI
- GMDN Term
- Resectoscope FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 876.1500 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
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Resectoscope
Gyrus ACMI by Gyrus Acmi, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Cleared under the same submission
K990628 also covers:
- GYRUS ACMI — Gyrus Acmi, Inc.
- GYRUS ACMI — Gyrus Acmi, Inc.
- GYRUS ACMI — Gyrus Acmi, Inc.
- GYRUS ACMI — Gyrus Acmi, Inc.
- GYRUS AMCI — Gyrus Acmi, Inc.
- Gyrus ACMI — Gyrus Acmi, Inc.
- Gyrus ACMI — Gyrus Acmi, Inc.
- Gyrus ACMI — Gyrus Acmi, Inc.
- Gyrus ACMI — Gyrus Acmi, Inc.
- Gyrus ACMI — Gyrus Acmi, Inc.
- Gyrus ACMI — Gyrus Acmi, Inc.
- Gyrus ACMI — Gyrus Acmi, Inc.
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 II | Pending data |
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Manufacturer
- Manufacturer
- Gyrus Acmi, Inc.
Sources (1)
- FDA UDI 4b9dd663-cc56-4815-b024-0d23319466af 34 fields · synced May 30, 2026