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KIM (Knotless Incontinence Mesh)

FDA UDI

Class II (US FDA UDI)

by Desarrollo E Investigacion Medica Aragonesa Sl

Identity

Trade Name
KIM (Knotless Incontinence Mesh) FDA UDI
Generic Name
Female stress urinary incontinence surgical mesh-sling, synthetic polymer FDA UDI
Model / Reference
KIM01/OID5 FDA UDI

Identifiers

Primary DI / UDI-DI
08437007606065 FDA UDI
FDA Product Code
OTN FDA UDI
GMDN Term
Female stress urinary incontinence surgical mesh-sling, synthetic polymer FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.3300 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: Female stress urinary incontinence surgical mesh-sling, synthetic polymer

KIM (Knotless Incontinence Mesh) by Desarrollo E Investigacion Medica Aragonesa Sl — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Female stress urinary incontinence surgical mesh-sling, synthetic polymer.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Desarrollo E Investigacion Medica Aragonesa Sl

Sources (1)

  • FDA UDI 933cc0d8-d313-4bd8-bf0f-8a807a501cb7 32 fields · synced May 31, 2026