Identity
- Trade Name
- Towako FDA UDI
- Generic Name
- Body aspiration needle, single-use FDA UDI
- Device Name
- Transmyometrial, Embryo Transfer Set FDA UDI
- Model / Reference
- G18742 FDA UDI
- Description
- Transmyometrial, Embryo Transfer Set FDA UDI
Identifiers
- Catalog Number
- K-TTET-19-32.5-TOWAKO FDA UDI
- Primary DI / UDI-DI
- 00827002187429 FDA UDI
- 510(k) Number
- K983595 FDA UDI
- FDA Product Code
- MQF FDA UDI
- GMDN Term
- Body aspiration needle, single-use FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 884.6110 FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
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
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Towako by William A. Cook Australia Pty. Ltd. — Class II — 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 II | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- William A. Cook Australia Pty. Ltd.
Sources (1)
- FDA UDI 64fea6e9-33af-4033-b856-285e88b3f20f 38 fields · synced Jun 6, 2026