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SURGICEL SNoW

FDA UDI

Class III (US FDA UDI)

by Ethicon Inc.

Identity

Trade Name
SURGICEL SNoW FDA UDI
Generic Name
Plant polysaccharide haemostatic agent, bioabsorbable FDA UDI
Device Name
Surgicel Absorbable Hemostat, Structured Non-Woven Fabric FDA UDI
Model / Reference
2083 FDA UDI
Description
Surgicel Absorbable Hemostat, Structured Non-Woven Fabric FDA UDI

Identifiers

Catalog Number
2083 FDA UDI
Primary DI / UDI-DI
10705031063600 FDA UDI
FDA Product Code
LMG FDA UDI
GMDN Term
Plant polysaccharide haemostatic agent, bioabsorbable FDA UDI

Classification

Device Class
Class III FDA UDI
Regulation Number
878.4490 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: Plant polysaccharide haemostatic agent, bioabsorbable

SURGICEL SNoW by Ethicon Inc. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Plant polysaccharide haemostatic agent, bioabsorbable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Ethicon Inc.

Sources (1)

  • FDA UDI af45f008-9d29-4728-81d1-a78b57a5d0f0 37 fields · synced May 30, 2026