Identity
- Trade Name
- Instrapac FDA UDI
- Generic Name
- Intrauterine device removal hook, single-use FDA UDI
- Device Name
- Instrapac IUD Hook 31cm/12in X 20 FDA UDI
- Model / Reference
- 7024 FDA UDI
- Description
- Instrapac IUD Hook 31cm/12in X 20 FDA UDI
Identifiers
- Catalog Number
- 7024 FDA UDI
- Primary DI / UDI-DI
- 05010058070240 FDA UDI
- FDA Product Code
- HHF FDA UDI
- GMDN Term
- Intrauterine device removal hook, single-use FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 884.4530 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
Yes
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
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Dimensions & Sizes
- Size
- Length — 31 Centimeter FDA UDI
Category: Intrauterine device removal hook, single-use
Instrapac by Robinson Healthcare Limited — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Intrauterine device removal hook, single-use.
- PremierPro — SVS LLC · Class I
- Instrapac — ROBINSON HEALTHCARE LIMITED · Class I
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Robinson Healthcare Limited
Sources (1)
- FDA UDI c836d454-1fc5-45b5-aea8-165b7e394c69 37 fields · synced May 30, 2026