← Back to catalogue

Phasix

FDA UDI

Class II (US FDA UDI)

by Davol Inc.

Identity

Trade Name
Phasix FDA UDI
Generic Name
Extra-gynaecological surgical mesh, synthetic polymer, bioabsorbable FDA UDI
Device Name
Phasix ST Mesh, 20 cm x 25 cm (8" x 10"), Rectangle FDA UDI
Model / Reference
1202025 FDA UDI
Description
Phasix ST Mesh, 20 cm x 25 cm (8" x 10"), Rectangle FDA UDI

Identifiers

Catalog Number
1202025 FDA UDI
Primary DI / UDI-DI
00801741095368 FDA UDI
FDA Product Code
FTL FDA UDI
OOD FDA UDI
OWT FDA UDI
GMDN Term
Extra-gynaecological surgical mesh, synthetic polymer, bioabsorbable 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

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

Dimensions & Sizes

Size
Length — 20 Centimeter FDA UDI
Width — 25 Centimeter FDA UDI

Category: Extra-gynaecological surgical mesh, synthetic polymer, bioabsorbable

Phasix by Davol Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Extra-gynaecological surgical mesh, synthetic polymer, bioabsorbable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Davol Inc.

Sources (1)

  • FDA UDI 1f8ad538-6a6d-4ac5-97dd-828c1dbc41a1 37 fields · synced May 30, 2026