Identity
- Trade Name
- USA Elite FDA UDI
- Generic Name
- Laparoscopic access cannula seal reducer, single-use FDA UDI
- Device Name
- ACMI USA Elite System and USA Series Self Sealing Seals (Black) (6/PK) FDA UDI
- Model / Reference
- S-AWE-S FDA UDI
- Description
- ACMI USA Elite System and USA Series Self Sealing Seals (Black) (6/PK) FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00821925038653 FDA UDI
- FDA Product Code
- FFY FDA UDI
- GMDN Term
- Laparoscopic access cannula seal reducer, single-use FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 876.1500 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
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
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Laparoscopic access cannula seal reducer, single-use
USA Elite by Gyrus Acmi, Inc. — 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
- Gyrus Acmi, Inc.
Sources (1)
- FDA UDI 909b7d1a-1fa7-416a-a9ee-5012ce7b9c86 33 fields · synced Jun 1, 2026