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Ethibond Excel

FDA UDI

Class I (US FDA UDI)

by Ethicon Inc.

Identity

Trade Name
ETHIBOND EXCEL FDA UDI
Generic Name
Polyester suture, non-bioabsorbable, multifilament FDA UDI
Device Name
White Braided Polyester, Nonabsorbable Surgical Suture FDA UDI
Model / Reference
D8150 FDA UDI
Description
White Braided Polyester, Nonabsorbable Surgical Suture FDA UDI

Identifiers

Catalog Number
D8150 FDA UDI
Primary DI / UDI-DI
10705031029309 FDA UDI
FDA Product Code
GEA FDA UDI
GMDN Term
Polyester suture, non-bioabsorbable, multifilament FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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

Category: Polyester suture, non-bioabsorbable, multifilament

Ethibond Excel by Ethicon Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Polyester suture, non-bioabsorbable, multifilament.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Ethicon Inc.

Sources (1)

  • FDA UDI fdec26db-bb65-415c-a735-9e98cab1dd8a 35 fields · synced Jun 1, 2026