Identity
- Trade Name
- Hemorrhoid Ligator FDA UDI
- Generic Name
- Haemorrhoid ligator FDA UDI
- Device Name
- Adler Hemorrhoid Ligator FDA UDI
- Model / Reference
- AL8000 FDA UDI
- Description
- Adler Hemorrhoid Ligator FDA UDI
Identifiers
- Catalog Number
- AL8000 FDA UDI
- Primary DI / UDI-DI
- 00850348007335 FDA UDI
- FDA Product Code
- FHN FDA UDI
- GMDN Term
- Haemorrhoid ligator FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 876.4400 FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
Yes
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
Yes
FDA UDI
Hemorrhoid Ligator by Adler MicroMed, Inc. — Class II — 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 II | Pending data |
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Manufacturer
- Manufacturer
- Adler MicroMed, Inc.
Sources (1)
- FDA UDI 13d12800-738e-45cf-948e-17e9a3e86817 35 fields · synced May 30, 2026