Identity
- Trade Name
- AM12M FDA UDI
- Generic Name
- Electrocardiographic lead set, reusable FDA UDI
- Device Name
- Wired Acquisition System cleared with Surveyor S12/S19 Monitor FDA UDI
- Model / Reference
- 41000-037-51 FDA UDI
- Description
- Wired Acquisition System cleared with Surveyor S12/S19 Monitor FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00812345029673 FDA UDI
- 510(k) Number
- K123556 FDA UDI
- FDA Product Code
- MHX FDA UDI
- GMDN Term
- Electrocardiographic lead set, reusable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.1025 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
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Electrocardiographic lead set, reusable
Am12m by Mortara Instrument, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Electrocardiographic lead set, reusable.
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- Unimed — Unimed Medical Supplies, Inc. · Class II
- Unimed — Unimed Medical Supplies, Inc. · Class II
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- Unimed — Unimed Medical Supplies, Inc. · Class II
Cleared under the same submission
K123556 also covers:
- AM12M — MORTARA INSTRUMENT, INC.
- AM12M — MORTARA INSTRUMENT, INC.
- Surveyor S12 — MORTARA INSTRUMENT, INC.
- Surveyor S12 — MORTARA INSTRUMENT, INC.
- Surveyor S12 — MORTARA INSTRUMENT, INC.
- Surveyor S12 — MORTARA INSTRUMENT, INC.
- Surveyor S12 — MORTARA INSTRUMENT, INC.
- Surveyor S12 — MORTARA INSTRUMENT, INC.
- Surveyor S12 — MORTARA INSTRUMENT, INC.
- Surveyor S12 — MORTARA INSTRUMENT, INC.
- Surveyor S12 — MORTARA INSTRUMENT, INC.
- Surveyor S12 — MORTARA INSTRUMENT, 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
- Mortara Instrument, Inc.
Sources (1)
- FDA UDI b694a1b5-e0a1-44bf-92ff-fdfee67e8a69 36 fields · synced May 30, 2026