← Back to catalogue

SV BOLSTER Medium

FDA UDI

Class I (US FDA UDI)

by Sun-Scientific Inc.

Identity

Trade Name
SV BOLSTER Medium FDA UDI
Generic Name
Exudate-absorbent dressing, non-gel, non-antimicrobial FDA UDI
Device Name
SAPHENOUS VEIN COMPRESSION FOAM DRESSING WITH AIR BOLSTER MEDIUM FDA UDI
Model / Reference
SP2355 FDA UDI
Description
SAPHENOUS VEIN COMPRESSION FOAM DRESSING WITH AIR BOLSTER MEDIUM FDA UDI

Identifiers

Catalog Number
SP2355 FDA UDI
Primary DI / UDI-DI
00856525007136 FDA UDI
510(k) Number
K070457 FDA UDI
FDA Product Code
NAC FDA UDI
GMDN Term
Exudate-absorbent dressing, non-gel, non-antimicrobial FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4018 FDA UDI
Commercial Distribution
Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

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

Yes

FDA UDI

SV BOLSTER Medium by Sun-Scientific Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Cleared under the same submission

K070457 also covers:

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
Sun-Scientific Inc.

Sources (1)

  • FDA UDI feac492d-d05a-4915-89c3-87e320f64126 37 fields · synced May 30, 2026