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3M™ Precise™

FDA UDI

Class I (US FDA UDI)

by 3m Company

Identity

Trade Name
3M™ Precise™ FDA UDI
Generic Name
Skin staple remover, single-use FDA UDI
Device Name
3M™ Precise™ Disposable Skin Staple Remover, Scissor-Style SR-3 FDA UDI
Model / Reference
SR-3 FDA UDI
Description
3M™ Precise™ Disposable Skin Staple Remover, Scissor-Style SR-3 FDA UDI

Identifiers

Catalog Number
SR-3 FDA UDI
Primary DI / UDI-DI
30707387027392 FDA UDI
FDA Product Code
GDT FDA UDI
GMDN Term
Skin staple remover, single-use 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 staple remover, single-use

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

Similar devices

Also classified as Skin staple remover, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
3m Company

Sources (1)

  • FDA UDI 1fd5ab4b-06c1-4317-84b8-f4024487dd9a 35 fields · synced Jun 6, 2026