Identity
- Trade Name
- SCANLAN® Ligator FDA UDI
- Generic Name
- Haemorrhoid ligator FDA UDI
- Device Name
- SCANLAN® Replacement Cone for McGivney Hemorrhoidal Ligator EUDAMEDReplacement Cone for Hemorrhoidal Ligator FDA UDI
- Model / Reference
- 2813-00 EUDAMED1001-50-C FDA UDI
- Description
- Replacement Cone for Hemorrhoidal Ligator FDA UDI
Identifiers
- Catalog Number
- 1001-50-C FDA UDI
- Primary DI / UDI-DI
- 00846159025903 EUDAMEDFDA UDI
- Basic UDI-DI
- B-00846159025903 EUDAMED
- FDA Product Code
- FHN FDA UDI
- EMDN Code
- L031102 EXPLORATION PROBES, REUSABLE EUDAMED
- GMDN Term
- Haemorrhoid ligator FDA UDI
Classification
- Device Class
- Class I EUDAMEDClass II FDA UDI
- Regulation Number
- 876.4400 FDA UDI
- Market of Registration
- Netherlands EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
EUDAMEDFDA UDI
Single Use
No
FDA UDI
Implantable
No
EUDAMEDFDA UDI
Reusable
No
EUDAMED
Contains Latex
No
EUDAMEDFDA UDI
Reprocessed
No
EUDAMED
CMR Substance
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Endocrine Disruptor
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
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
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Haemorrhoid ligator
SCANLAN® Ligator by Scanlan International Inc — Class II — MDD, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS
Similar devices
Also classified as Haemorrhoid ligator.
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- Surgical Direct — SURGICAL DIRECT, INC. · Class I
- Millennium — AVALIGN TECHNOLOGIES, Inc. · Class II
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Unknown
MDD
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | MDD | — | Class II | Unknown |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Scanlan International Inc
Sources (2)
- FDA UDI 517ebf2b-376c-46ba-b87d-acdcec1d4aa2 35 fields · synced Jul 15, 2026
- EUDAMED b779f248-596d-4e27-b831-f7b03dc011b8 61 fields · synced Jul 15, 2026