Identity
- Trade Name
- GYRUS ACMI FDA UDI
- Generic Name
- General-purpose surgical scissors, reusable FDA UDI
- Device Name
- SCISSORS, CURVED SHARP/SHARP OVERALL LENGTH 115 MM (4.5") FDA UDI
- Model / Reference
- 550007 FDA UDI
- Description
- SCISSORS, CURVED SHARP/SHARP OVERALL LENGTH 115 MM (4.5") FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00821925020139 FDA UDI
- FDA Product Code
- HNF FDA UDI
- GMDN Term
- General-purpose surgical scissors, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 886.4350 FDA UDI
- Commercial Distribution
- Not 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
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Gyrus Acmi by Gyrus Acmi, 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
- Gyrus Acmi, Inc.
Sources (1)
- FDA UDI ac29b578-80a8-40bb-99fa-4861be34d869 34 fields · synced May 31, 2026