Identity
- Trade Name
- Perclose™ ProStyle™ FDA UDI
- Generic Name
- Femoral vessel suture implantation set FDA UDI
- Device Name
- Perclose™ ProStyle™ Suture-Mediated Closure and Repair System FDA UDI
- Model / Reference
- 12773-03 FDA UDI
- Description
- Perclose™ ProStyle™ Suture-Mediated Closure and Repair System FDA UDI
Identifiers
- Catalog Number
- 12773-03 FDA UDI
- Primary DI / UDI-DI
- 08717648235184 FDA UDI
- FDA Product Code
- MGB FDA UDI
- GMDN Term
- Femoral vessel suture implantation set FDA UDI
Classification
- Device Class
- Class III FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
Yes
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
No
FDA UDI
Category: Femoral vessel suture implantation set
Perclose™ ProStyle™ by Abbott Vascular — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Femoral vessel suture implantation set.
- Prostar™ — Abbott Vascular · Class III
- Perclose ProGlide™ — Abbott Vascular · Class III
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 III | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Abbott Vascular
Sources (1)
- FDA UDI 0992436f-54c2-4ca5-a46b-d8e95e99b620 36 fields · synced May 30, 2026