Identity
- Trade Name
- Thumper FDA UDI
- Generic Name
- Cardiac resuscitator, pneumatic FDA UDI
- Device Name
- External Cardiac Compressor - Model 1007CCMII FDA UDI
- Model / Reference
- 1007CCMII FDA UDI
- Description
- External Cardiac Compressor - Model 1007CCMII FDA UDI
Identifiers
- Catalog Number
- 15350 FDA UDI
- Primary DI / UDI-DI
- 00860682000107 FDA UDI
- 510(k) Number
- K972525 FDA UDI
- FDA Product Code
- DRM FDA UDI
- GMDN Term
- Cardiac resuscitator, pneumatic FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.5200 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
Yes
FDA UDI
MR Safe FDA UDI
Category: Cardiac resuscitator, pneumatic
Thumper by Michigan Instruments — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Cardiac resuscitator, pneumatic.
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
- Michigan Instruments
Sources (1)
- FDA UDI 863ba9a8-47b4-44f5-ba59-1f37b4d34894 36 fields · synced Jun 8, 2026