Identity
- Trade Name
- JEDMED FDA UDI
- Generic Name
- Lacrimal tube insertion hook/pusher FDA UDI
- Device Name
- HOOK CRAWFORD FDA UDI
- Model / Reference
- 28-0186 FDA UDI
- Description
- HOOK CRAWFORD FDA UDI
Identifiers
- Catalog Number
- 28-0186 FDA UDI
- Primary DI / UDI-DI
- M6332801860 FDA UDI
- FDA Product Code
- OKS FDA UDI
- GMDN Term
- Lacrimal tube insertion hook/pusher FDA UDI
Classification
- Device Class
- U FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Lacrimal tube insertion hook/pusher
Jedmed by JEDMED Instrument Company — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Lacrimal tube insertion hook/pusher.
- Stephens Instruments — KRISHNA IMPORTS INC · Class I
- Visitec® — Beaver-Visitec International, Inc. · Class I
- Lacrimal Probe — Katena Products, Inc. · Class I
- JEDMED — JEDMED Instrument Company · U
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 U | Pending data |
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Manufacturer
- Manufacturer
- JEDMED Instrument Company
Sources (1)
- FDA UDI a17b0798-3809-46bb-b59c-f9d329ba679a 34 fields · synced Jun 6, 2026