Identity
- Trade Name
- TRANSWAAG FDA UDI
- Generic Name
- Blood weighing scale FDA UDI
- Device Name
- Blood mixing and weighing device FDA UDI
- Model / Reference
- TRANSWAAG PRO FDA UDI
- Description
- Blood mixing and weighing device FDA UDI
Identifiers
- Catalog Number
- 97.8700.105 FDA UDI
- Primary DI / UDI-DI
- 04028339620139 FDA UDI
- FDA Product Code
- KSQ FDA UDI
- GMDN Term
- Blood weighing scale FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 864.9195 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
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
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: Blood weighing scale
Transwaag by Transmed Medizintechnik GmbH & Co. KG — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Blood weighing scale.
- Triton — Stryker Corp. · Class I
- TRITON — Stryker Corp. · Class I
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 |
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Manufacturer
- Manufacturer
- Transmed Medizintechnik GmbH & Co. KG
Sources (1)
- FDA UDI e34aaec5-6cfd-43d2-a2df-d42f04a240e9 35 fields · synced May 30, 2026