Identity
- Trade Name
- Leica Biosystems Ariol Cable, stage sensor FDA UDI
- Generic Name
- Electrical mains power extension cable FDA UDI
- Device Name
- Leica Biosystems Ariol Cable, stage sensor FDA UDI
- Model / Reference
- 23ASLSP030 FDA UDI
- Description
- Leica Biosystems Ariol Cable, stage sensor FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00849832011576 FDA UDI
- FDA Product Code
- NQN FDA UDI
- GMDN Term
- Electrical mains power extension cable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 864.1860 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
No
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Electrical mains power extension cable
Leica Biosystems Ariol Cable, stage sensor by Leica Biosystems Richmond, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Electrical mains power extension cable.
- 320 S37, SY, BE, 2L, 2LD, BE(9&13), 36" — CURBELL MEDICAL PRODUCTS, INC. · Class II
- 3701 S37, 1TO1, STANDARD, 90°, 144" — CURBELL MEDICAL PRODUCTS, INC. · Class II
- ADAPTOR, 1, P808, (2)S808, IN, TT — CURBELL MEDICAL PRODUCTS, INC. · Class II
- P1500, S102, 6", NO DP, CURBELL — CURBELL MEDICAL PRODUCTS, INC. · Class II
- 103, 102 P37, BE & NURSE, STKR — CURBELL MEDICAL PRODUCTS, INC. · Class II
- 3701 P37, 1TO1, STND, 72", ALT. THUMBSCREWS — CURBELL MEDICAL PRODUCTS, INC. · Class II
- ADAPTOR, 12, P1802, S3701, MNTG BRKT — CURBELL MEDICAL PRODUCTS, INC. · Class II
- 307, 102 P37, E2, BE, 1L — CURBELL MEDICAL PRODUCTS, INC. · Class II
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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Leica Biosystems Richmond, Inc.
Sources (1)
- FDA UDI c1b74e68-f12e-4e40-8286-fb444d62cb0f 36 fields · synced May 30, 2026