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Sign in to claim this brandTIDI PRODUCTS, LLC
United States·US-MF-000012287
Last updated September 17, 2026
Information
- Country
- United States
- Address
- 570, Enterprise Drive, Neenah, United States
- Website
- tidiproducts.com
- —
- —
- [email protected]
- Phone
- 1-920-751-4300 x 4009
- PRRC Contact
- Chris Rahn
- EUDAMED SRN
- US-MF-000012287
- FDA FEI Number
- 2182318
- DUNS Number
- —
Catalogue (2730)
Page 42 of 55| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Tidishield | 21040 | FDA UDI | Class I | Active |
| Bone Foam | 25192 | FDA UDI | Class II | Unknown |
| Tidi | 141 | FDA UDI | Class II | Unknown |
| Preferred Surgical Products | 28694 | FDA UDI | Class II | Unknown |
| Tidi | 9104 | FDA UDI | Class II | Unknown |
| Tidi | 9425 | FDA UDI | Class II | Unknown |
| Tidi | 105-SCB | FDA UDI | Class II | Unknown |
| GE Healthcare | 30801 | FDA UDI | Class II | Unknown |
| Tidi | 9012-D | FDA UDI | Class II | Active |
| tidi | 32452 | FDA UDI | Class I | Unknown |
| Tidi | 32719 | FDA UDI | Class II | Unknown |
| Vital Care | 29863 | FDA UDI | Class II | Unknown |
| Dornier MedTech Europe | 30415 | FDA UDI | Class II | Unknown |
| TIDIShield | MICK-P416 | FDA UDI | Class II | Active |
| Tidi | 32999 | FDA UDI | Class II | Unknown |
| Tidi | 145-20 | FDA UDI | Class II | Unknown |
| Tidi | 32066 | FDA UDI | Class II | Unknown |
| Tidi | 20435 | FDA UDI | Class II | Unknown |
| Tidi | 30940 | FDA UDI | Class II | Unknown |
| Dornier MedTech Europe | 30415 | FDA UDI | Class II | Unknown |
| C-Armor | 5536 | FDA UDI | Class II | Unknown |
| Grip-Lok | 3309MCS-TA-2 | FDA UDI | Class I | Active |
| Tidi | 960176 | FDA UDI | Class II | Active |
| Tidi | 161-8 | FDA UDI | Class II | Unknown |
| Tidi | 817-V | FDA UDI | Class II | Unknown |
| Tidi | 27191 | FDA UDI | Class II | Unknown |
| Tidi | 9073 | FDA UDI | Class II | Unknown |
| Medi-Inn | MICK-PC748BE | FDA UDI | Class II | Active |
| Transmedics | 32674 | FDA UDI | Class II | Unknown |
| Tidi | 193 | FDA UDI | Class II | Unknown |
| TIDIShield | CFI-6022 | FDA UDI | Class II | Unknown |
| Neurologica | 30253 | FDA UDI | Class II | Unknown |
| Zero Gravity | ZGAV-XL | FDA UDI | Class I | Active |
| Oec | 31883 | FDA UDI | Class II | Active |
| AquaGuard | 50011-RPK | FDA UDI | Class I | Active |
| Tidi | 33134 | FDA UDI | Class II | Unknown |
| Gems | 20929F | FDA UDI | Class II | Unknown |
| Tidi | 27538 | FDA UDI | Class II | Unknown |
| SteriGear | 28016 | FDA UDI | Class II | Unknown |
| Tidi | CFI-821 | FDA UDI | Class II | Active |
| Grip-Lok | 3300M-10PK | FDA UDI | Class I | Unknown |
| Zero Gravity | ZG48 | FDA UDI | Class I | Active |
| Tidi | 33040 | FDA UDI | Class II | Unknown |
| Tidi | 22640 | FDA UDI | Class II | Unknown |
| Tidi | 173 | FDA UDI | Class II | Unknown |
| Tidi | 26785 | FDA UDI | Class II | Unknown |
| Tidi | 168 | FDA UDI | Class II | Unknown |
| Tidi | 33121 | FDA UDI | Class II | Unknown |
| Tidi | 23708 | FDA UDI | Class II | Unknown |
| TIDIShield | 5535 | FDA UDI | Class II | Unknown |
Related Companies
Authorised Representatives
- MDSS GmbH DE
Importers
Not available yet.
Notified Bodies
Not available yet.
Authorities
Not available yet.
FDA Recalls (1)
Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.
| Date | Recall No. | Class | Status | Reason |
|---|---|---|---|---|
| Apr 12, 2019 | Z-0194-2020 | — | terminated | Not meeting design specifications. |