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Anchorsure

FDA UDI

Class II (US FDA UDI)

by Desarrollo E Investigacion Medica Aragonesa Sl

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

Similar devices

Also classified as Soft-tissue/mesh anchor, non-bioabsorbable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI a78d5b9f-6b20-491c-95fb-61741c228c01 32 fields · synced May 30, 2026