← Back to catalogue

Sbh

FDA UDI

Class I (US FDA UDI)

by SBH Surgical

Identity

Trade Name
SBH FDA UDI
Generic Name
Nail clippers, single-use FDA UDI
Device Name
Sterile, Single-Use, Ruskin Liston Bone Forceps, 6”/15cm, Straight FDA UDI
Model / Reference
Single Use - SBH 636560 FDA UDI
Description
Sterile, Single-Use, Ruskin Liston Bone Forceps, 6”/15cm, Straight FDA UDI

Identifiers

Catalog Number
SBH 636560 FDA UDI
Primary DI / UDI-DI
00850068304028 FDA UDI
FDA Product Code
KDC FDA UDI
GMDN Term
Nail clippers, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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

No

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

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Nail clippers, single-use

Sbh by SBH Surgical — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Nail clippers, single-use.

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
SBH Surgical

Sources (1)

  • FDA UDI e5f67340-8ea3-478c-98f5-89ccac638315 35 fields · synced Jun 1, 2026