← Back to catalogue

Monoplus

FDA UDI

Class II (US FDA UDI)

by B Braun Surgical Sa

Identity

Trade Name
Monoplus FDA UDI
Generic Name
Polyester suture, bioabsorbable, monofilament, non-antimicrobial FDA UDI
Device Name
MONOPLUS VIOLET 0 (3,5) 90CM HS26S(M) FDA UDI
Model / Reference
G0024018 FDA UDI
Description
MONOPLUS VIOLET 0 (3,5) 90CM HS26S(M) FDA UDI

Identifiers

Catalog Number
G0024018 FDA UDI
Primary DI / UDI-DI
04046964551970 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
Not 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

Dimensions & Sizes

Size
Length — 90.00 Centimeter FDA UDI

Monoplus by B Braun Surgical Sa — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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
B Braun Surgical Sa

Sources (1)

  • FDA UDI 0fde3104-6c50-4276-bf23-9ec8e5aa8304 37 fields · synced May 31, 2026