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WEGO-Polypropylene Nonabsorbable Surgical Suture With Needle

FDA UDI

Class II (US FDA UDI)

by Foosin Medical Supplies, Inc.

Identity

Trade Name
WEGO-Polypropylene Nonabsorbable Surgical Suture With Needle FDA UDI
Generic Name
Polyolefin/fluoropolymer suture, monofilament FDA UDI
Model / Reference
P33193 FDA UDI

Identifiers

Primary DI / UDI-DI
06941813671107 FDA UDI
510(k) Number
K080684 FDA UDI
FDA Product Code
GAW FDA UDI
GMDN Term
Polyolefin/fluoropolymer suture, monofilament FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.5010 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

Category: Polyolefin/fluoropolymer suture, monofilament

WEGO-Polypropylene Nonabsorbable Surgical Suture With Needle by Foosin Medical Supplies, Inc. — Class II — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Polyolefin/fluoropolymer suture, monofilament.

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 7d2294ee-2c4d-4866-bc47-293133c8c875 33 fields · synced May 30, 2026