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Peri-Strips Dry with Veritas Collagen Matrix Circular
FDA UDIClass II (US FDA UDI)
Identity
- Trade Name
- Peri-Strips Dry with Veritas Collagen Matrix Circular FDA UDI
- Generic Name
- Staple line-reinforcement strip FDA UDI
- Device Name
- Peri-Strips Dry with Veritas Collagen Matrix (PSD-V) Circular Staple Line Reinforcement is prepared from dehydrated bovine pericardium procured from cattle under 30 months of age in the United States. The packaging contains two loading units w/buttress material, one for the anvil and one for the cartridge side of the stapler. The packaging also includes one cartridge cone to aid atraumatic advancement of the stapler into the surgical site, and one tube of PSD Gel to create a temporary bond between the buttress and the surgical stapler until the stapler is positioned and fired. FDA UDI
- Model / Reference
- PSD21EV FDA UDI
- Description
- Peri-Strips Dry with Veritas Collagen Matrix (PSD-V) Circular Staple Line Reinforcement is prepared from dehydrated bovine pericardium procured from cattle under 30 months of age in the United States. The packaging contains two loading units w/buttress material, one for the anvil and one for the cartridge side of the stapler. The packaging also includes one cartridge cone to aid atraumatic advancement of the stapler into the surgical site, and one tube of PSD Gel to create a temporary bond between the buttress and the surgical stapler until the stapler is positioned and fired. FDA UDI
Identifiers
- Catalog Number
- PSD21EVBIO FDA UDI
- Primary DI / UDI-DI
- 00085412531281 FDA UDI
- FDA Product Code
- FTM FDA UDI
- GMDN Term
- Staple line-reinforcement strip FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 878.3300 FDA UDI
- Commercial Distribution
- Not 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
Peri-Strips Dry with Veritas Collagen Matrix Circular by Synovis Life Technologies, Inc. — Class II — FDA UDI — listed in FDA GUDID
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 |
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Manufacturer
- Manufacturer
- Synovis Life Technologies, Inc.
Sources (1)
- FDA UDI 0bc32dc8-6e36-44fc-9b93-ae5f6545f0be 37 fields · synced May 30, 2026