← Back to catalogue

Arista

FDA UDI

Class III (US FDA UDI)

by Davol Inc.

Identity

Trade Name
ARISTA FDA UDI
Generic Name
Plant polysaccharide haemostatic agent, bioabsorbable FDA UDI
Device Name
Arista AH Absorbable Hemostatic Particles, 1g bellows container FDA UDI
Model / Reference
SM0005-USA FDA UDI
Description
Arista AH Absorbable Hemostatic Particles, 1g bellows container FDA UDI

Identifiers

Catalog Number
SM0005-USA FDA UDI
Primary DI / UDI-DI
00801741044120 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

Dimensions & Sizes

Size
Weight — 1 Gram FDA UDI

Category: Plant polysaccharide haemostatic agent, bioabsorbable

Arista by Davol Inc. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Plant polysaccharide haemostatic agent, bioabsorbable.

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
Davol Inc.

Sources (1)

  • FDA UDI a81f460a-0f11-48c7-8db6-aa7ba52a9265 37 fields · synced May 30, 2026