Identity
- Trade Name
- PeroSupport.tec FDA UDI
- Generic Name
- Ankle/foot orthosis FDA UDI
- Device Name
- PeroSupport.pro, Ankle-Foot-Orthosis with additional calve stabilisation, made of carbon-prepreg, dynamic, right, shoe size 42 - 45 FDA UDI
- Model / Reference
- 197R6/R3 FDA UDI
- Description
- PeroSupport.pro, Ankle-Foot-Orthosis with additional calve stabilisation, made of carbon-prepreg, dynamic, right, shoe size 42 - 45 FDA UDI
Identifiers
- Catalog Number
- 197R6/R3 FDA UDI
- Primary DI / UDI-DI
- 04048817530569 FDA UDI
- FDA Product Code
- OHI FDA UDI
- GMDN Term
- Ankle/foot orthosis FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 890.3475 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
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Ankle/foot orthosis
PeroSupport.tec by Streifeneder ortho.production GmbH — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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
- Streifeneder ortho.production GmbH
Sources (1)
- FDA UDI 4b1b4b72-b1a7-4178-be81-2d49d86f8b20 35 fields · synced May 30, 2026