Identity
- Trade Name
- BMM FDA UDI
- Generic Name
- Ambulatory monitoring/recording system transceiver/cable FDA UDI
- Model / Reference
- Rev A FDA UDI
Identifiers
- Primary DI / UDI-DI
- 11968525357367 FDA UDI
- FDA Product Code
- KMI FDA UDI
- GMDN Term
- Ambulatory monitoring/recording system transceiver/cable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 880.2400 FDA UDI
- Commercial Distribution
- Not 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
No
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
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Bmm by Atlas Lift Tech, Inc. — Class I — 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 I | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Atlas Lift Tech, Inc.
Sources (1)
- FDA UDI 637dc5ec-a88b-489e-bb91-14f29e3e2d80 33 fields · synced May 30, 2026