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Dagrofil

FDA UDI

Class II (US FDA UDI)

by B Braun Surgical Sa

Identity

Trade Name
Dagrofil FDA UDI
Generic Name
Polyester suture, non-bioabsorbable, multifilament FDA UDI
Device Name
DAGROFIL GREEN 2/0 (3) 3X45CM FDA UDI
Model / Reference
C0346268 FDA UDI
Description
DAGROFIL GREEN 2/0 (3) 3X45CM FDA UDI

Identifiers

Catalog Number
C0346268 FDA UDI
Primary DI / UDI-DI
04038653798421 FDA UDI
FDA Product Code
GAT FDA UDI
GMDN Term
Polyester suture, non-bioabsorbable, multifilament FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.5000 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 — 45.00 Centimeter FDA UDI

Dagrofil 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

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Manufacturer

Manufacturer
B Braun Surgical Sa

Sources (1)

  • FDA UDI 0fba5be8-1552-4580-abd7-47aa8ad42c74 37 fields · synced May 31, 2026