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IJS-E (Twin)

FDA UDI

Class II (US FDA UDI)

by Skeletal Dynamics L.l.c.

Identity

Trade Name
IJS-E (Twin) FDA UDI
Generic Name
Fluted surgical drill bit, single-use FDA UDI
Device Name
Drill, 3.7mm x 30mm FDA UDI
Model / Reference
IJS FDA UDI
Description
Drill, 3.7mm x 30mm FDA UDI

Identifiers

Catalog Number
DRLL-SSC-37030 FDA UDI
Primary DI / UDI-DI
00841506114323 FDA UDI
FDA Product Code
OZI FDA UDI
LXT FDA UDI
GMDN Term
Fluted surgical drill bit, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3030 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

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

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Fluted surgical drill bit, single-use

IJS-E (Twin) by Skeletal Dynamics L.l.c. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Fluted surgical drill bit, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 85502aee-d62d-436c-bdc3-4354b4afed78 35 fields · synced May 31, 2026