Identity
- Trade Name
- ACMI ADAPTOR FDA UDI
- Generic Name
- Endoscopic light source adaptor FDA UDI
- Model / Reference
- 906137 FDA UDI
Identifiers
- Catalog Number
- 906137 FDA UDI
- Primary DI / UDI-DI
- 00880304407916 FDA UDI
- 510(k) Number
- K920800 FDA UDI
- FDA Product Code
- HRX FDA UDI
- GMDN Term
- Endoscopic light source adaptor FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.1100 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: Endoscopic light source adaptor
Acmi Adaptor by Biomet Orthopedics, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Endoscopic light source adaptor.
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- TELE PACK — Karl Storz GmbH & Co. KG · Class II
- FENTEX — FENTEX medical GmbH · Class I
- Gimmi — Gimmi GmbH · Class II
- CONMED — Conmed Corporation · Class I
- FENTEX — FENTEX medical GmbH · Class I
Cleared under the same submission
K920800 also covers:
- 3.5MM DOUBLE TOOTH — Biomet Orthopedics, Inc.
- 3.5MM FULL RADIUS — Biomet Orthopedics, Inc.
- 3.5MM MENISCUS CUTTER — Biomet Orthopedics, Inc.
- 3.5MM MICROSHARP FULL RADIUS — Biomet Orthopedics, Inc.
- 4.5MM BARREL ROTOR BUR — Biomet Orthopedics, Inc.
- 4.5MM DOUBLE TOOTH — Biomet Orthopedics, Inc.
- 4.5MM FULL RADIUS — Biomet Orthopedics, Inc.
- 4.5MM MENISCUS CUTTER — Biomet Orthopedics, Inc.
- 4.5MM MICROSHARP FULL RADIUS — Biomet Orthopedics, Inc.
- 4.5MM ROUND ABRADER — Biomet Orthopedics, Inc.
- 4.5MM ROUND ROTOR BUR — Biomet Orthopedics, Inc.
- 4MM X 9FT. LIGHT CABLE — Biomet Orthopedics, 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
- Biomet Orthopedics, Inc.
Sources (1)
- FDA UDI 9b24a920-a376-4dbb-b957-ff01dd827ece 35 fields · synced Jun 8, 2026