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3M™ Snap™

FDA UDI

Class II (US FDA UDI)

by Kci Usa, Inc.

Identity

Trade Name
3M™ Snap™ FDA UDI
Generic Name
Negative-pressure wound therapy system dressing set FDA UDI
Device Name
3M™ Snap™ Plus Therapy Strap, STPAMP, Medium, 1 Each/Case FDA UDI
Model / Reference
STPAMP FDA UDI
Description
3M™ Snap™ Plus Therapy Strap, STPAMP, Medium, 1 Each/Case FDA UDI

Identifiers

Catalog Number
STPAMP FDA UDI
Primary DI / UDI-DI
00849554008694 FDA UDI
FDA Product Code
OKO FDA UDI
GMDN Term
Negative-pressure wound therapy system dressing set FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4683 FDA UDI
Commercial Distribution
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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Negative-pressure wound therapy system dressing set

3M™ Snap™ by Kci Usa, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Negative-pressure wound therapy system dressing set.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Kci Usa, Inc.

Sources (1)

  • FDA UDI 886f1d1a-0009-463c-b2d5-e35224cd12b8 35 fields · synced May 31, 2026