← Back to catalogue

3M™ Precise™

FDA UDI

Class I (US FDA UDI)

by 3m Company

Identity

Trade Name
3M™ Precise™ FDA UDI
Generic Name
Skin stapler/staple, non-bioabsorbable FDA UDI
Device Name
3M™ Precise™ Vista Disposable Skin Stapler 3995 FDA UDI
Model / Reference
3995 FDA UDI
Description
3M™ Precise™ Vista Disposable Skin Stapler 3995 FDA UDI

Identifiers

Catalog Number
3995 FDA UDI
Primary DI / UDI-DI
30707387092291 FDA UDI
FDA Product Code
GDT FDA UDI
GMDN Term
Skin stapler/staple, non-bioabsorbable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4760 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Skin stapler/staple, non-bioabsorbable

3M™ Precise™ by 3m Company — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Skin stapler/staple, non-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
3m Company

Sources (1)

  • FDA UDI 63d80af6-06a7-4fab-856e-2def63f33fc1 35 fields · synced Jun 7, 2026