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Safil

FDA UDI

Class II (US FDA UDI)

by B Braun Surgical Sa

Identity

Trade Name
Safil FDA UDI
Generic Name
Polyester suture, bioabsorbable, multifilament, non-antimicrobial FDA UDI
Device Name
SAFIL VIOLET 2 (5) 2X70CM FDA UDI
Model / Reference
X1038410 FDA UDI
Description
SAFIL VIOLET 2 (5) 2X70CM FDA UDI

Identifiers

Catalog Number
X1038410 FDA UDI
Primary DI / UDI-DI
04038653966004 FDA UDI
FDA Product Code
GAM FDA UDI
GMDN Term
Polyester suture, bioabsorbable, multifilament, non-antimicrobial FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4493 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 — 70.0 Centimeter FDA UDI

Safil 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 559fd5fa-18fc-4354-9669-ca116e5b3a90 37 fields · synced May 31, 2026