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Pds

FDA UDI

Class II (US FDA UDI)

by Ethicon Inc.

Identity

Trade Name
PDS FDA UDI
Generic Name
Polyester suture, bioabsorbable, monofilament, non-antimicrobial FDA UDI
Device Name
Undyed Monofilament (Polydioxanone), Absorbable Synthetic Surgical Suture FDA UDI
Model / Reference
Z824G FDA UDI
Description
Undyed Monofilament (Polydioxanone), Absorbable Synthetic Surgical Suture FDA UDI

Identifiers

Catalog Number
Z824G FDA UDI
Primary DI / UDI-DI
10705031061804 FDA UDI
FDA Product Code
NEW FDA UDI
GMDN Term
Polyester suture, bioabsorbable, monofilament, non-antimicrobial FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4840 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

No

FDA UDI
MRI Safety
MR Safe FDA UDI

Category: Polyester suture, bioabsorbable, monofilament, non-antimicrobial

Pds by Ethicon Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Polyester suture, bioabsorbable, monofilament, non-antimicrobial.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Ethicon Inc.

Sources (1)

  • FDA UDI a18bd6ab-662c-42ca-bbfa-fa7d1cc16183 35 fields · synced Jun 1, 2026