Identity
- Trade Name
- Anchorsure FDA UDI
- Generic Name
- Soft-tissue/mesh anchor, non-bioabsorbable FDA UDI
- Model / Reference
- A-SURE FDA UDI
Identifiers
- Primary DI / UDI-DI
- 08437007606904 FDA UDI
- FDA Product Code
- PBQ FDA UDI
- GMDN Term
- Soft-tissue/mesh anchor, non-bioabsorbable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 884.4530 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
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
Yes
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Soft-tissue/mesh anchor, non-bioabsorbable
Anchorsure by Desarrollo E Investigacion Medica Aragonesa Sl — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Soft-tissue/mesh anchor, non-bioabsorbable.
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- MectaScrew PEEK — Medacta International · Class II
- FiberStitch™ Implant, Reverse Curve with two Polyester Implants and 2-0 FiberWir — T.A.G MEDICAL PRODUCTS AGRICULTURAL COOPERATIVE ASSOCIATION · Class II
- Heli-FX™ Thoracic EndoAnchor™ System — MEDTRONIC VASCULAR, INC. · Class II
- JUGGERSTITCH™ — Biomet Orthopedics, Inc. · Class II
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
- Desarrollo E Investigacion Medica Aragonesa Sl
Sources (1)
- FDA UDI a78d5b9f-6b20-491c-95fb-61741c228c01 32 fields · synced May 30, 2026