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Instant Detacher

FDA UDI

Class II (US FDA UDI)

by Micro Therapeutics, Inc.

Identity

Trade Name
Instant Detacher FDA UDI
Generic Name
Vascular implant detacher, electronic, single-use FDA UDI
Device Name
Detacher ID-1-5 V02 FDA UDI
Model / Reference
ID-1-5 FDA UDI
Description
Detacher ID-1-5 V02 FDA UDI

Identifiers

Primary DI / UDI-DI
00763000290702 FDA UDI
510(k) Number
K060747 FDA UDI
FDA Product Code
KRD FDA UDI
HCG FDA UDI
GMDN Term
Vascular implant detacher, electronic, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.3300 FDA UDI
882.5950 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

No

FDA UDI

Dimensions & Sizes

Size
Depth — 6.6 Inch FDA UDI
Length — 9.9 Inch FDA UDI
Height — 4.0 Inch FDA UDI

Category: Vascular implant detacher, electronic, single-use

Instant Detacher by Micro Therapeutics, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Vascular implant detacher, electronic, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Micro Therapeutics, Inc.

Sources (1)

  • FDA UDI ed9517a3-fc96-4aa2-9220-367c43412c2b 37 fields · synced May 31, 2026