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SnugFit ASA

FDA UDI

Class II (US FDA UDI)

by Medacta International

Identity

Trade Name
SnugFit ASA FDA UDI
Generic Name
Soft-tissue/mesh anchor, non-bioabsorbable FDA UDI
Device Name
SnugFit ASA Size1 2xUSP#2 (bl+w/bl) Short FDA UDI
Model / Reference
05.11.072 FDA UDI
Description
SnugFit ASA Size1 2xUSP#2 (bl+w/bl) Short FDA UDI

Identifiers

Primary DI / UDI-DI
07630542778872 FDA UDI
510(k) Number
K251933 FDA UDI
FDA Product Code
MBI FDA UDI
GMDN Term
Soft-tissue/mesh anchor, non-bioabsorbable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3040 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

Yes

FDA UDI
MRI Safety
MR Safe FDA UDI

Category: Soft-tissue/mesh anchor, non-bioabsorbable

SnugFit ASA by Medacta International — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI a785279a-a2b0-44f4-b31a-6f0ead9180d4 34 fields · synced Jun 8, 2026